Effect of dexamethasone in patients with ARDS and COVID-19 – prospective, multi-centre, open-label, parallel-group, randomised controlled trial (REMED trial): A structured summary of a study protocol for a randomised controlled trial

Objectives The primary objective of this study is to test the hypothesis that administration of dexamethasone 20 mg is superior to a 6 mg dose in adult patients with moderate or severe ARDS due to confirmed COVID-19. The secondary objective is to investigate the efficacy and safety of dexamethasone 20 mg versus dexamethasone 6 mg. The exploratory objective of this study is to assess long-term consequences on mortality and quality of life at 180 and 360 days. Trial design REMED is a prospective, phase II, open-label, randomised controlled trial testing superiority of dexamethasone 20 mg vs 6 mg. The trial aims to be pragmatic, i.e. designed to evaluate the effectiveness of the intervention in conditions that are close to real-life routine clinical practice. Participants The study is multi-centre and will be conducted in the intensive care units (ICUs) of ten university hospitals in the Czech Republic. Inclusion criteria Subjects will be eligible for the trial if they meet all of the following criteria: 1. Adult (≥18 years of age) at time of enrolment; 2. Present COVID-19 (infection confirmed by RT-PCR or antigen testing); 3. Intubation/mechanical ventilation or ongoing high-flow nasal cannula (HFNC) oxygen therapy; 4. Moderate or severe ARDS according to Berlin criteria:  • Moderate – PaO2/FiO2 100–200 mmHg;  • Severe – PaO2/FiO2 < 100 mmHg; 5. Admission to ICU in the last 24 hours. Exclusion criteria Subjects will not be eligible for the trial if they meet any of the following criteria: 1. Known allergy/hypersensitivity to dexamethasone or excipients of the investigational medicinal product (e.g. parabens, benzyl alcohol); 2. Fulfilled criteria for ARDS for ≥14 days at enrolment; 3. Pregnancy or breastfeeding; 4. Unwillingness to comply with contraception measurements from enrolment until at least 1 week after the last dose of dexamethasone (sexual abstinence is considered an adequate contraception method); 5. End-of-life decision or patient is expected to die within next 24 hours; 6. Decision not to intubate or ceilings of care in place; 7. Immunosuppression and/or immunosuppressive drugs in medical history:  a) Systemic immunosuppressive drugs or chemotherapy in the past 30 days;  b) Systemic corticosteroid use before hospitalization;  c) Any dose of dexamethasone during the present hospital stay for COVID-19 for ≥5 days before enrolment;  d) Systemic corticosteroids during present hospital stay for conditions other than COVID-19 (e.g. septic shock); 8. Current haematological or generalized solid malignancy; 9. Any contraindication for corticosteroid administration, e.g.  • intractable hyperglycaemia;  • active gastrointestinal bleeding;  • adrenal gland disorders;  • presence of superinfection diagnosed with locally established clinical and laboratory criteria without adequate antimicrobial treatment; 10. Cardiac arrest before ICU admission; 11. Participation in another interventional trial in the last 30 days. Intervention and comparator Dexamethasone solution for injection/infusion is the investigational medicinal product as well as the comparator. The trial will assess two doses, 20 mg (investigational) vs 6 mg (comparator). Patients in the intervention group will receive dexamethasone 20 mg intravenously once daily on day 1–5, followed by dexamethasone 10 mg intravenously once daily on day 6–10. Patients in the control group will receive dexamethasone 6 mg day 1–10. All authorized medicinal products containing dexamethasone in the form of solution for i.v. injection/infusion can be used. Main outcomes Primary endpoint: Number of ventilator-free days (VFDs) at 28 days after randomisation, defined as being alive and free from mechanical ventilation. Secondary endpoints a) Mortality from any cause at 60 days after randomisation; b) Dynamics of inflammatory marker (C-Reactive Protein, CRP) change from Day 1 to Day 14; c) WHO Clinical Progression Scale at Day 14; d) Adverse events related to corticosteroids (new infections, new thrombotic complications) until Day 28 or hospital discharge; e) Independence at 90 days after randomisation assessed by Barthel Index. The long-term outcomes of this study are to assess long-term consequences on mortality and quality of life at 180 and 360 days through telephone structured interviews using the Barthel Index. Randomisation Randomisation will be carried out within the electronic case report form (eCRF) by the stratified permuted block randomisation method. Allocation sequences will be prepared by a statistician independent of the study team. Allocation to the treatment arm of an individual patient will not be available to the investigators before completion of the whole randomisation process. The following stratification factors will be applied: • Age <65 and ≥ 65; • Charlson Comorbidity index (CCI) <3 and ≥3; • CRP <150 mg/L and ≥150 mg/L • Trial centre. Patients will be randomised in a 1 : 1 ratio into one of the two treatment arms. Randomisation through the eCRF will be available 24 hours every day. Blinding (masking) This is an open-label trial in which the participants and the study staff will be aware of the allocated intervention. Blinded pre-planned statistical analysis will be performed. Numbers to be randomised (sample size) The sample size is calculated to detect the difference of 3 VFDs at 28 days (primary efficacy endpoint) between the two treatment arms with a two-sided type I error of 0.05 and power of 80%. Based on data from a multi-centre randomised controlled trial in COVID-19 ARDS patients in Brazil and a multi-centre observational study from French and Belgian ICUs regarding moderate to severe ARDS related to COVID-19, investigators assumed a standard deviation of VFD at 28 days as 9. Using these assumptions, a total of 142 patients per treatment arm would be needed. After adjustment for a drop-out rate, 150 per treatment arm (300 patients per study) will be enrolled. Trial Status This is protocol version 1.1, 15.01.2021. The trial is due to start on 2 February 2021 and recruitment is expected to be completed by December 2021. Trial registration The study protocol was registered on EudraCT No.:2020-005887-70, and on December 11, 2020 on ClinicalTrials.gov (Title: Effect of Two Different Doses of Dexamethasone in Patients With ARDS and COVID-19 (REMED)) Identifier: NCT04663555 with a last update posted on February 1, 2021. Full protocol The full protocol (version 1.1) is attached as an additional file, accessible from the Trials website (Additional file 1). In the interest of expediting dissemination of this material, the standard formatting has been eliminated; this Letter serves as a summary of the key elements of the full protocol. Supplementary Information The online version contains supplementary material available at 10.1186/s13063-021-05116-9.


STATEMENT
The following persons undertake to conduct the study "Effect of dexamethasone in patients with ARDS and COVID-19prospective, multi-centre, open-label, parallel-group, randomized controlled trial (REMED trial)" according to this protocol and in compliance with applicable national and international requirements, mainly:

Rationale and up-to-date evidence
Systemic corticosteroids have the potential to limit hyperinflammatory response by modulating the immune system. This effect is mediated mainly by binding to the glucocorticoid receptor (GR) α (2). Their effectiveness was proved in heterogeneous ARDS patients recently (3).
In patients with COVID-19 pneumonia in need for oxygen therapy or mechanical ventilation, dexamethasone 6 mg per day is currently recommended. This therapy is mandated by the results of RECOVERY trial (4). After this trial was published, three randomized trials comparing hydrocortisone (5,6) or dexamethasone (7) against placebo were stopped prematurely. All these studies were included in the subsequent individual patients' data (IPD) meta-analysis (8). However, the dose of 6 mg of dexamethasone is currently being reappraised.
The aforementioned study in non-COVID-19 ARDS patients (3) used 20 mg of dexamethasone per day, which is roughly equivalent to the methylprednisolone regimen (1 mg/kg/day) studied in early severe ARDS patients (9). Only these moderate doses (80-100 mg of methylprednisolone, equivalent to 15-19 mg of dexamethasone) have the full potential to modulate the immune response by saturating GRα receptors (2). Importantly, prematurely stopped CoDEX trial (7) comparing dexamethasone against placebo in COVID-19 ARDS patients used an initial daily dose of 20 mg of dexamethasone versus placebo.
In the light of these facts, 6 mg of dexamethasone given to COVID-19 patients with different severity of illness (WHO classification group 5-10) may miss important therapeutic potential or may prevent a potential deleterious effects of a full dose therapeutic corticosteroid. Authors hypothesize that the patients with moderate to severe ARDS undergoing mechanical ventilation may benefit from higher doses of dexamethasone (3,7,9).

Anticipated risks and benefits
There may or may not benefit from a higher dose of dexamethasone in the improvement of the clinical outcomes of an individual participant. However, there is a potential benefit to society from the participation in this study resulting from insights gained about the dexamethasone use and posology. The potential risks of participating in this study are those associated with dexamethasone use, i.e. known adverse effects of potent glucocorticoids.

Primary objective(s) and endpoint(s)
The primary objective of this study is to test the hypothesis that administration of dexamethasone 20 mg is superior over 6 mg in adult patients with moderate or severe ARDS due to confirmed COVID-19.
Primary endpoint: Number of ventilator-free days (VFDs) at 28 days after randomization.
VFDs were defined according to recent recommendations (10): • Day 0 is the day of randomization

Secondary objective(s) and endpoint(s)
The secondary objective is to investigate the efficacy and safety of dexamethasone 20 mg versus dexamethasone 6 mg.

Exploratory objective(s) and endpoint(s)
The exploratory objective of this study is to assess long-term consequences on mortality and quality of life at 180 and 360 days.

TRIAL DESIGN
REMED is a prospective phase II open-label randomized controlled trial testing superiority of dexamethasone 20 mg vs 6 mg. The study is multi-centre and will be conducted in intensive care units (ICUs) of university hospitals in the Czech Republic. The trial aims to be pragmatic, i.e. designed to evaluate the effectiveness of the intervention in conditions that are very close to the real-life routine clinical practice. Dexamethasone will be administered once daily 9 / 29 intravenously for 10 days. 300 participants will be enrolled and followed up for 360 days after randomization.

Exclusion criteria
Subjects will not be eligible for the trial if they meet any of the following criteria: 1. Known allergy/hypersensitivity to dexamethasone or excipients of the investigational medicinal product (e.g. parabens, benzyl alcohol); 2. Fulfilled criteria for ARDS for ≥ 14 days at enrolment; 3. Pregnancy or breastfeeding; 4. Unwillingness to comply with contraception measurements from the enrolment to at least 1 week after the last dose of dexamethasone (sexual abstinence is considered as the adequate contraception method); 5. End-of-life decision or patient is expected to die within next 24 hours; 6. Decision not to intubate or ceilings of treatment in place; 7. Immunosuppression and/or immunosuppressive drugs in medical history: a) Systemic immunosuppressive drugs or chemotherapy in the past 30 days; b) Systemic corticosteroids use before hospitalization; c) Any dose of dexamethasone during the present hospital stay for COVID-19 for more than (≥) last 5 days before enrolment; d) Systemic corticosteroids during present hospital stay for other conditions than COVID-19 (e.g. septic shock); 8. Present haematological or generalized solid malignancy; 9. Any of contraindications of corticosteroids, e.g.
• intractable hyperglycaemia; • active gastrointestinal bleeding; • adrenal gland disorders; • a presence of superinfection diagnosed with locally established clinical and laboratory criteria without adequate antimicrobial treatment; 10. Cardiac arrest before ICU admission; 11. Participation in another interventional trial in the last 30 days.

Randomization and stratification
Randomization will be carried out within the electronic case report form (eCRF) by the stratified permuted block randomization method. The allocation sequences will be prepared by a statistician independent of the study team. Allocation to the treatment arm of an individual patient will not be available to the investigators before the completion of the whole randomization process. Following stratification factors will be applied: • Age < 65 and ≥ 65 (12); • Charlson Comorbidity index (CCI; APPENDIX B Assessment tools, scores, and scales, Chapter 14.2) < 3 and ≥ 3; • CRP < 150 mg/L and ≥ 150 mg/L • Trial centre.
Patients will be randomized in 1 : 1 ratio in one of the two treatment arms. Randomization through eCRF will be available 24 hours every day.

Blinding
This is an open-label trial, in which the participants and the study staff will learn about the allocated intervention. Blinded pre-planned statistical analysis will be performed (13) according to Chapter 8.

Enrolment stopping rules
Enrolment of new subjects into the trial will be stopped if any of the following is encountered until the sponsor determines if it is safe for the trial to continue enrolment: • Death that is related to dexamethasone; • SAE or SUSAR (see Chapter 7.7) that is related to dexamethasone during 28 days postadministration; • Emergence of new data that may lead to the trial becoming unethical. This may be merely due to safety concerns of the interventional group (e.g., if harm is reported by other trials). • After the interim analysis, the Steering committee will review primary outcomes and the summary of adverse events in both arms whilst still blinded to treatment allocation. The enrolment can be stopped if the following criteria are fulfilled: a) There is a significant difference in the primary outcome at p < 0.01 between the arms. b) Futility: The futility criterion is not binding for the Steering committee. Based on available data, the study statistician calculates the probability of being able to reject the null hypothesis with achieving the target number of subjects and the probability of type II error made by stopping the trial prematurely.

Premature termination of participation in the trial
Reasons for early termination of a patient's participation include: • Withdrawal of informed consent (subject's decision to withdraw for any reason); • Important deviation in the process of informed consent (Chapter 10.1); • Life-threatening adverse reaction to dexamethasone at the discretion of the investigator;

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• Newly-emerged pregnancy of a participant after the enrolment; Subjects can terminate their participation prematurely at any time at their request for any reason, but they must notify the investigator. The investigator must contact the sponsor to report the premature discontinuation.
The investigator must: • Instruct the participant about the right on early termination of participation; • Assure him/her that the end of participation will not affect the attitude of the physician, or further treatment and its quality; • Ask for discussing this decision with the investigator in advance; • Make a note in the patient's medical records and eCRF about the date of early termination of participation.
The sponsor reserves the right to discontinue the study at any time if there is a significant safety concern (e.g. grade 4 adverse reactions to dexamethasone), or insufficient recruitment despite intensified efforts to enrol patients, or if repeated poor study documentation occurs at a site. The trial can be discontinued by the decision of the regulatory authority or ethics committee, as well.

STUDY TREATMENT Dexamethasone (ATC code: H02AB02)
Dexamethasone solution for injection/infusion is the investigational medicinal product as well as the comparator. The trial will assess two doses, 20 mg (investigational) vs 6 mg (comparator).
All authorized medicinal products containing dexamethasone in the form of solution for i.v. injection/infusion can be used.

Qualitative and quantitative composition
Active pharmaceutical ingredient: Dexamethasone sodium phosphate (4 mg/mL) Excipients: Excipients differ in various dexamethasone solutions for inj./inf. Please see the SmPC of the medicinal product you are using. Several excipients have known biological effects (e.g., allergic reactions): methylparaben, propylparaben, benzyl alcohol. Allergy or hypersensitivity to dexamethasone or excipients is an exclusion criterion (Chapter 4.2).

Pharmaceutical form and route of administration
Solution for injection/infusion; intravenous administration

Other information
Detailed pharmacological profile of the drug, including information on the mechanism of action, contraindications, drug interactions, adverse effects and others can be found in the SmPC.

Packaging and labelling
The medicinal product will be labelled in accordance with applicable legislation. Specimen of the labelling can be found in APPENDIX A, Chapter 14.1.

Delivery and storage
The medicinal product containing dexamethasone will be ordered regularly by trial sites' hospital pharmacies and taken from the Czech market. It will be stored up to 30°C in the secondary package to keep it from the light according to the SmPC recommendations.

Dosing schedule
Patients in the intervention group will receive dexamethasone 20 mg intravenously once daily on day 1-5, followed by dexamethasone 10 mg intravenously once daily on day 6-10.
Patients in the control group will receive dexamethasone 6 mg day 1-10.

Dose modification and delays
For this study, no dose modification or delays are possible.
Previous treatment with any dose of dexamethasone for more than (≥) 5 days during the present hospital stay for COVID-19 is an exclusion criterion (Chapter 4.2, point 6c). If the study subject is treated with any dose of dexamethasone for less than 5 days before the enrolment, he/she can be enrolled, and there will be no changes in the duration of study drug administration.

Permitted concomitant medication
Study participants will receive the best standard of care according to local protocols and national guidelines, including the state-of-the-art anti-infective and adjunctive treatment of COVID-19, sedation and delirium management, physiotherapy, ventilator, and haemodynamic management.
All chronic medication prescribed to the patient before the enrolment is permitted to continue with the exceptions defined in Chapter 4.2 (point 6) and Chapter 5.7. All necessary medication needed during the trial is allowed with exceptions defined in Chapter 5.7.

Restricted concomitant medication
Systemic corticosteroids other than dexamethasone are restricted, as well as other investigational medicinal products currently tested for the treatment of COVID-19 (e.g., investigational antivirals, or monoclonal antibodies). Remdesivir is not considered as an investigational drug, as it has already been authorized.
Concomitant treatment with potent inhibitors of CYP3A increases the risk of systemic adverse effects of dexamethasone. In cases where benefits of such treatment do not overweight this increased risk, combination with strong inhibitors of CYP3A is considered restricted.
Concomitant use of potent inducers of CYP3A decreases the effect of dexamethasone, which may then bias the results. In cases where benefits of such treatment do not overweight this risk of bias, combination with potent inducers of CYP3A is considered restricted.
Detailed information on drug interactions could be found in SmPC.

Screening of eligible patients
Patients admitted to ICU of each centre will be screened daily for the eligibility, and all the patients will be recorded in the screening log of eCRF. For patients with the completion of consent, appropriate enrolment information will be recorded to eCRF and only after all required information are provided the randomization and allocation will proceed.
For details on obtaining the informed consent see Chapter 10.1.

Overview of medical care about the study participant
Patient in both arms will receive the best standard of care. General supportive care guided by official recommendations and local protocols will be given, as described in Chapter 5.6.
The centres are encouraged to follow appropriate antibiotic stewardship practices, e.g. guidelines for hospital-acquired and ventilator-associated pneumonia (VAP/HAP) management (15

Clinical examinations and assessments
During the trial course, subjects will be monitored during hospitalization and after discharge. A summary of scheduled procedures is outlined in Chapter 6.4. For a graphic summary see Table 1.

Day 2
• Administration of dexamethasone according to the allocation to treatment arms • Inflammatory markers (CRP; other markers e.g., procalcitonine, presepsin, interleukin-6 at the discretion of each centre) • COV-HI assessment (APPENDIX B, Chapter 14.2.4)based on Day 2 CRP level.

Day 3 to Day 10
• Administration of dexamethasone according to the allocation to treatment arms • Inflammatory markers (CRP; other markers e.g., procalcitonine, presepsin, interleukin-6 at the discretion of each centre)

Day 1 to Day 28 / ICU discharge (whichever comes first)
• Checking adverse events and adverse reactions (with special interest in newly emerged infections and new thrombotic complications) • Ventilatory status, i.e. use of a mechanical ventilator or other ventilation/oxygen support

Biological samples
Blood samples will be taken following local practice and analysed in the respective clinical laboratory facility of the trial centre. No other biological specimens will be obtained or stored in this trial.

Assessment tools, scores, and scales
The following tools will be used during the trial and are described in APPENDIX B Assessment tools, scores, and scales, Chapter 14.

SAFETY ASSESSMENTS
Before the start of the clinical trial, all Investigators will undergo training in pharmacovigilance requirements and obtain detailed written instructions for recording and reporting of AEs. These instructions for pharmacovigilance will be part of the Investigator's Site File.

Definitions (according to the Directive 2001/20/EG)
For clinical trials, effective legislation has introduced the following definitions.

Adverse event AE
Any untoward medical occurrence in a patient or clinical trial subject administered a medicinal product and which does not necessarily have a causal relationship with this treatment.

Adverse drug reaction ADR
All untoward and unintended responses to an investigational medicinal product related to any dose administered

Serious adverse event SAE
A serious adverse event/reaction is any untoward medical occurrence or effect that at any dose: • Results in death; • Is life-threatening; • Requires hospitalization or extension of existing hospitalization; • Results in persistent or significant disability or incapacity; • Is a congenital anomaly or birth defect.

Serious adverse reaction SADR
Unexpected adverse reaction UADR Adverse reaction, the nature, severity, or outcome of which is not consistent with the product information (SmPC) Suspected unexpected serious adverse reaction

SUSAR
Any suspected adverse reaction related to the study treatment that is both serious and unexpected.

AE surveillance, recording and documentation
AE could be diseases or symptoms which occur or worsen after the enrolment of a patient in the clinical trial. All AEs need to be documented, no matter if the investigator suspects a causal connection to the study medication. AE will be monitored and documented from the day of giving informed consent until the end of participation in the study (i.e., Day 360).
Subjects will be instructed to report any AEs that they experience to the investigator. The investigator should actively ask about AEs.
Each AE should be described, documented in the eCRF, and evaluated to determine: • Seriousness (see Chapter 7.4); • Severity (see Chapter 7.5); • Causality, i.e. relation to the study medication (see Chapter 7.6.); • Duration (start and end dates or whether it continues).
• Action taken (no action taken; study medication discontinued; prolongation of the ongoing hospitalization; administration of a drug etc.) AE needs to be followed until its resolution, i.e. until it subsides, stabilizes, becomes chronic, or the subject dies.
If AE fulfils the criteria of SAE, a separate form must be completed besides the standard eCRF record (see Chapter 7.7).
AEs will be recorded according to the Medical Dictionary for Regulatory Activities (MedDRA). The most recent MedDRA version at the start of the study will be used.

Treatment of AE
A patient with an AE must receive appropriate therapy. The investigator may decide to discontinue the study medication. The patient will remain under medical supervision until the investigator believes that the AE has been resolved.

Assessment of seriousness
AE is considered serious if it fulfils the definition in Chapter 7.1.
Some situations can be considered as SAE even if they do not fulfil the criteria of the definition. These are important medical events that may not be immediately life-threatening, or result in death, or hospitalization but may jeopardize the subject, or may require intervention to prevent one of the other outcomes listed in the definition above. These should also be considered SAEe.g., allergic bronchospasm, convulsions, or other states requiring treatment.
If AE fulfils the criteria of SAE, a separate Serious Adverse Event Form must be completed and sent to the sponsor. For the procedure see Chapter 7.7.
In this clinical trial, the following SAE are excluded from the notification requirement: • SAE which occurs after enrolment (i.e., after giving informed consent), but before the study medication was initiated; • Hospitalization(s) planned before the enrolment; • Death not related to the dexamethasone use.

Assessment of intensity (severity)
The intensity (severity) of an AE should be evaluated according to these 5 categories:

Grade 1
AE is asymptomatic or mildly symptomatic, requires only observation, no medical intervention Grade 2 AE with medium intensity, requires local, non-invasive, or small-scale treatment Grade 3 AE is medically significant, requires hospitalization or extension of ongoing hospitalization, but it is not directly life-threatening

Assessments of causality
To assess the relation between administration of the study medication and the AE, the following definitions apply: • Related -The event is known to occur with the study medication, there is a reasonable possibility that the study medication caused the AE, or there is a temporal relationship between the study medication and AE. Reasonable possibility means that there is evidence to suggest a causal relationship between the study medication and the AE.
• Not related -There is not a reasonable possibility that the administration of the study medication caused the AE, there is no temporal relationship between the study medication and AE onset, or an alternate aetiology has been established.

Reporting of SAE and SUSAR
If at that point all required information is not available, succeeding records will be sent by the investigator. Sponsor will check the notification completeness and formal plausibility. If required, queries will be made and followed up.
In the case of death, a copy of the autopsy record should be added. If the death of the subject complies with the definition of SUSAR (see Chapter 7.1), it will be reported as SUSAR (see below).
Sponsor has full responsibility for the safety of the clinical trial. Further reporting of AEs to the competent authorities according to the legal requirements is the responsibility of the sponsor.

Follow-up
All SAEs should be followed until their resolution, i.e., they subside, stabilize, become chronic, or the subject dies followed. In case of early termination because of SAE occurrence, the subject should be followed until SAE resolution. All necessary extra visits will be recorded in the eCRF as "Unscheduled visits".
Follow-up information is sent using a new SAE Form stating that this is a follow-up to the previously reported SAE and giving the date of the original report. Within 24 hours of receipt of follow-up information, the investigator must update the SAE form and submit any supporting documentation (e.g., laboratory test reports, subject discharge summary, autopsy report etc.) The follow-up information should describe whether the event has resolved or continues, if and how it was treated and whether the patient continued or withdrew from trial participation.

Reporting of SUSAR
SAE related to the study medication fulfilling the criterion of unexpectedness (i.e., SUSAR) must be reported by the sponsor to the Ethics Committee and the EudraVigilance database (module EVCTM), at the latest 15 days after it becomes known. Sponsor will also inform all Investigators involved in the trial. Reporting to the EudraVigilance database will be performed via regulatory authority according to the agreement between the sponsor and the regulatory authority. In case of a fatal or life-threatening SUSAR, the sponsor will report all relevant Form (SAE Form). The blank forms are stored in the Investigator's Site File. The announcement will be done by e-mail: farmakovigilance@med.muni.cz AND nerusilova@med.muni.cz.

Pregnancy
Pregnant or breastfeeding women cannot be included in the study. Pregnancy testing (hCG, blood sample) is obligatory at enrolment in women of childbearing potential (i.e. from menarche to the onset of postmenopausal state). In case the information regarding menstrual cycle cannot be obtained from the patient due to her health or consciousness status, pregnancy testing is also necessary independently of patient's age. If statim hCG is not available at the moment of enrolment, investigators should perform urine pregnancy testing. Urine test strips will be supplied to the trial centres, where statim hCG is not available, e.g. on weekends or public holidays.
Participants, men and women, must comply with the required contraception measurements from the enrolment to at least 1 week after the last dose of dexamethasone. Sexual abstinence is considered as the adequate contraception method for this clinical trial. Newly-emerged pregnancy in the hospitalization phase of the trial is highly unlikely. However, if it is diagnosed, dexamethasone treatment must be stopped. If a participant becomes pregnant during the follow-up phase, she must inform the investigator.
Pregnancy should be followed by the investigator until completion. If it ends for any reason before the anticipated date, the investigator should notify the sponsor. At the completion of the pregnancy, the investigator will document the outcome of the pregnancy. If the outcome of the pregnancy meets the criteria for classification as SAE (e.g., spontaneous abortion, stillbirth, neonatal death, postpartum complication, or congenital anomaly), the investigator should follow the procedures for reporting an SAE (see Chapter 7.7).

STATISTICS
A separate Statistical Analysis Plan (SAP) and Statistical Interim Analysis Plan (SIAP) will be prepared to provide details on the approach to analyses. The SAP will be finalized before the interim database lock. All eventual deviations from the SAP will be described and justified in the relevant part of The Clinical Trial Report.

Sample size determination
The sample size was calculated to detect the difference of 3 VFDs at 28 days (primary efficacy endpoint) between the two treatment arms at two-sided type I error of 0.05 and power of 80%. Based on data from a multi-centre randomized controlled trial in COVID-19 ARDS patients in Brazil (7) and the multi-centre observational study from French and Belgian ICUs regarding moderate to severe ARDS related to COVID-19 (18), investigators assumed standard deviation of VFD at 28 days as SD=9. Using these assumptions, a total of 142 patients per

The Investigator should report the pregnancy to the Sponsor within 24 hours of learning of its occurrence using Pregnancy Form. This announcement will be done by e-mail: farmakovigilance@med.muni.cz AND nerusilova@med.muni.cz.
treatment arm would be needed, after adjustment for drop-out rate, 150 per treatment arm (300 patients per study) will be enrolled.

Analysis of efficacy
Primary efficacy endpoint (number of VFDs at day 28) will be calculated for both treatment arms separately with corresponding 95% confidence intervals. Comparison between arms will be based on parametric or non-parametric test (following the type of data distribution) and will be adjusted for relevant baseline covariates (stratification parameters) Secondary and exploratory efficacy endpoints will be analysed following the type of data (Chisquare test or Fisher's exact test for binary data and ANOVA or a non-parametric alternative tests for continuous and ordinal data, if appropriate).
The primary population for analysis of efficacy will be Intention-To-Treat population (ITT), and results will be confirmed on the Per-Protocol Population (PP).

Subgroup analysis
Pre-planned subgroup analysis will be performed regarding the primary outcome variable in the subgroups defined by the following criteria: No adjustments of p-values due to multiplicity are planned.

Analysis of safety
The safety will be analysed in all patients who received any dose of study treatment and provided at least one post-dose safety assessment (Safety Population). All adverse events will be coded and tabulated by system organ class and preferred term for individual events within each system organ class and will be presented in descending frequency. Adverse events will also be tabulated by severity and relationship to the study medication. Serious adverse events will be summarized separately.

Planned interim analysis
One interim analysis is planned for safety and efficacy evaluation after the primary outcome is known for the 150 th subject (50% of planned sample size). To control the overall level of type I error, the P value of 0.01 for interim analysis and 0.04 for the final analysis will be applied. All the details on stopping rules for interim analysis will be described in SIAP.
The interim analysis will be evaluated and decision about continuation of the study will be done by DMC.

Missing data
No imputation techniques for missing data will be applied.

DATA MANAGEMENT AND QUALITY ASSURANCE eCRF database
All participants will be assigned an identification code to ensure the pseudonymization of their data. The investigator will maintain a subject identification list for the trial centre (subject identification codes with the corresponding subject names) to enable records to be identified.
Trial data will be collected in eCRFs managed in electronic data capture system REDCap. Access to the database (username, password) will be granted by the study data manager, and the respective study staff will be trained for using it right and safely. The investigator is responsible for the data correctness, completeness, and filling in time. eCRF will be designed to generate queries on missing data or unusual data entries, which will be fed back to the study site investigators in regular intervals.

Trial documents, medical records
The sponsor, the trial site and study staff will handle the subject's personal and trial data according to the effective legislation regarding data protection. Any paper or electronic trial documents or data are confidential and must not be disclosed to the third persons. In the informed consent form, the participants are informed that their medical records can be provided only to the authorized monitors, auditors, or inspectors.
Medical records of the subjects will be retained in the trial site for 15 years (from the end of the clinical trial), so will be the relevant trial administrative documents at the sponsor's side.

Monitoring and auditing
The trial centre will be monitored according to the Monitoring plan. The objectives of the monitoring are to ensure that the trial participant's safety and rights are respected, that accurate, valid and complete data are collected, and that the trial is conducted in accordance with the trial protocol, the principles of GCP and national legislation. The investigator agrees that the monitor will regularly visit the trial centre and will be given appropriate support (e.g., the access to all necessary documents incl. patient's medical records). A report on the progress, findings and resolution of any discrepancies will be prepared from each monitoring visit. The investigator undertakes to read the monitoring report and to ensure that any possible discrepancies are corrected. Sponsor, Regulatory authority and Ethics committees have the right to inspect/audit the trial site. The investigator undertakes to co-operate will the inspectors/auditors.

Steering committee
The Steering Committee is constituted by all study investigators of the REMED trial. It is responsible for the development of the study protocol, continuous and final results interpretations and manuscripts preparation. The Steering Committee closely collaborates with independent Data monitoring committee and the sponsor.

Data monitoring committee
Members of data monitoring committee (DMC) are experts in intensive care medicine which are not involved in the REMED trial and an independent statistician. DMC is responsible for performing interim analysis and for providing recommendations to the Steering Committee and the sponsor regarding the safety and continuation of the trial based on evidence of possible significant differences between intervention and control group. Members of DMC are listed in a separate document.

ETHICAL ASPECTS
This trial will be conducted following the applicable legislation and requirements for good clinical practice according to the ICH E6(R2). Compliance with this standard provides public assurance that the rights, safety and well-being of trial participants are protected and that the clinical trial data are credible. All essential trial documents and their potential amendments will be submitted to the relevant Ethics committee and Regulatory authority for approval.

Informed consent procedure
The investigator assesses patient's ability to decide and extent of potential consciousness impairment based on GCS and other appropriate clinical measures (at discretion of the trial centre).

Fully conscious and oriented patients (GCS 15)
Patient with decision-making capacity will go through the standard procedure (informative interview with the investigator, written information for the patients, the possibility to ask questions, and adequate time to discuss with family and decide). If the patient wishes to participate, he/she will provide written prospective informed consent.

Patients with limited ability to decide (GCS 14 or 13)
Some patients may be limited in their decisional capacity due to their acute health status, or medication. Generally, if a patient understands simplified information and can communicate verbally, the simplified procedure of obtaining informed consent will be applied. The shortened (one-page) information sheet and consent form for signature will be used.
As soon as the patient regains full decisional capacity, he/she will be approached to provide consent with the continuation of his/her participation in the trial. Patients will be informed about the option to withdraw from the trial. Patients who decide to terminate their involvement can permit the sponsor to use the data collected, or they can ask for deleting all data collected. Both options will be presented to them.
If the patient does not regain a decisional capacity, the initial consent will remain valid.

Patients lacking the capacity to decide (GCS 12 or less)
It is expected that a significant proportion of screened patients will lack the capacity to provide informed consent due to severely altered consciousness, severe respiratory distress, or sedation necessary to facilitate mechanical ventilation. In this situation, the deferred consent policy will be applied. Such a patient will be enrolled after independent physician witnesses (in writing) that the patient cannot give his/her consent and fulfils eligibility criteria.
Patient's close person (spouse/partner, close relative, caregiver) will be informed about the patient's enrolment and the nature of the study. If possible and compliant with the epidemiological restrictions by the government, patient's close person will meet the investigator for an informative interview, to obtain the information leaflet, and to sign a confirmation that he/she was informed about the patient's participation in the trial.
As soon as the patient regains decisional capacity, he/she will be approached to provide consent with the continuation of his/her participation in the trial. Patients will be informed about the option to withdraw from the trial. Patients who decide to terminate their involvement can permit the sponsor to use the data collected, or they can ask for deleting all data collected. Both options will be presented to them.
If the patient does not regain a decisional capacity, the initial consent by an independent physician will remain valid.

Supervision of the informed consent procedure
The process of obtaining informed consent from a patient or an independent physician must always be appropriately documented by the investigator through valid forms and the patient's medical records, as well. The clinical trial monitor will check the process during the monitoring visits. Important deviations in the process will lead to the termination of the patient's participation in the trial.

Vulnerable population
Beside patients with diminished decision capacity, other specifically vulnerable participants (children, pregnant women, prisoners, refugees, institutionalized patients, patients with severe mental illnesses, etc.) will not be enrolled in this clinical trial.

PUBLICATION POLICY
Results of this clinical trial are planned to be published in the medical literature. Any publications must be approved by the sponsor and meet the quality requirements for current clinical research publications (e.g., CONSORT statement).

FINANCING AND INSURANCE
REMED is an investigator-initiated clinical trial. Funding will be granted from the project research infrastructure Czech Clinical Research Infrastructure Network CZECRIN (LM 2018128) and University Hospital Brno. Trial funders have no role in the study design, collection, analysis and interpretation of data. Investigators declare no financial or non-financial competing interest regarding the focus of this trial.
Mandatory insurance of the participants is arranged. The coverage for damages emerging from the participation in the clinical trial will be provided according to the applicable legal requirements.

SUPPLEMENTS/APPENDICES
APPENDIX A Specimen of labelling APPENDIX B Assessment tools, scores, and scales

APACHE II
The APACHE-II score provides an estimate of ICU mortality based on several laboratory values and patient signs taking both acute and chronic disease into account. The score consists of the following parameters: age, severe organ insufficiency/immunodeficiency, body temperature, mean arterial pressure, heart rate, RR, oxygenation, arterial pH, serum Na, K, creatinine, haematocrit, WBC, Glasgow coma scale. More information could be found here: https://www.mdcalc.com/apache-ii-score

Barthel index
The Barthel Index evaluates functional limitations in 10 activities of daily living: food intake, dressing, locomotion, stair walk, moving from bed to chair, personal hygiene, bathing, toilet use, and urine and stool continence. The assessment is performed by a healthcare professional. For details please see: https://www.uzis.cz/index.php?pg=registry-sber-dat-klasifikace--barthelove-test