Skip to main content

Fibromyalgia, milnacipran and experimental pain modulation: study protocol for a double blind randomized controlled trial

Abstract

Background

The prevalence of fibromyalgia increases worldwide and is characterized by widespread and chronic pain. Treatment is difficult and includes both drug and non-drug approaches. Milnacipran, an antidepressant, is used for fibromyalgia, with a possible beneficial effect on central pain modulation. Our hypothesis is that the efficacy of milnacipran in fibromyalgia depends on the performance of pain inhibitory controls.

Methods/design

A randomized, double blind, clinical trial (NCT01747044) with two parallel groups, in 48 women with fibromyalgia, is planned in the Clinical Pharmacology Center, University Hospital, Clermont-Ferrand, France. Conditioned pain modulation (estimated with thermal stimuli using a numeric pain rating scale), the primary endpoint measure, is evaluated before and one month after treatment with milnacipran or placebo. Secondary outcome measures include the predictability of pain descending pathways performance for milnacipran efficacy, tolerance and cognitive function. Data analysis is performed using mixed models; the tests are two-sided, with a type I error set at alpha = 0.05. Not only will this trial allow estimation of the beneficial effect of milnacipran on pain and on descending pain pathways but it will also evaluate whether the performance of this modulatory system could be predictive of its efficacy in alleviating pain.

Discussion

This method would allow clinicians to take a pro-active attitude by performing a rapid psychophysical test before starting milnacipran treatment and would avoid unnecessary prescription while preventing therapeutic failure in patients who often face this recurrent problem.

Trial registration

ClinicalTrials.gov NCT01747044.

Peer Review reports

Background

Fibromyalgia has a prevalence estimated at 2 to 5% of the general population in Europe [1] and in the United States of America [2] and is approximately seven times more common in women than in men [3]. Diagnostic criteria have been validated since 1990 by the American College of Rheumatology and have been enlarged in the 2010 revision to consider not only tender points but also cognitive problems and the extent of somatic symptoms [4]. The pathophysiology of fibromyalgia is uncertain but a dysfunction of descending pain inhibitory pathways [5-7] has been described as a cause or a consequence of the pathology [8]. These pathways originate in the brainstem and are involved in diffuse noxious inhibitory controls (DNICs) that are part of a central pain modulatory system relying on spinal and supraspinal mechanisms [9]. This pain modulatory system can be easily triggered and studied in experimental settings [10,11] using the conditioned pain modulation test, where the administration of two simultaneous painful stimuli typically results in pain inhibition [12,13]. Stimulation of DNICs is commonly used to evaluate any impairment of descending pain modulation.

Antidepressants have a mechanism of action that involves a number of neuromediators (serotonin, noradrenaline) within the brain-brainstem-spinal-cord axis and affects pain descending pathways [14]. Duloxetine and milnacipran are serotonin and norepinephrine reuptake inhibitors and have been approved for treatment of fibromyalgia by the Food and Drug Administration [15-17] for their analgesic properties [14]. Experiments on the safety, tolerability, and clinical benefits of long-term milnacipran use in patients with fibromyalgia have shown good results [18]. A review of four double blind studies focused on the efficacy of milnacipran in fibromyalgia [18]: a substantial improvement on global status was observed and more than 30% pain relief was obtained but only in 40% patients.

Considering this large variability in response to milnacipran, it is expected that a number of patients will have no alleviation of pain: it would be beneficial for the patient to be able to predict the efficacy of milnacipran in pain associated with fibromyalgia before the prescription of the drug. It would also be important to evaluate cognitive function, which is frequently impaired in chronic pain [19]. This information would enable prescription of the drug to be avoided if no efficacy is expected, and would avoid therapeutic failure in patients who often stop their treatment because of lack of efficacy. Such a predictive approach has been performed with duloxetine in another pathology, painful diabetic neuropathy [13], where the authors have shown that pain alleviation may be predicted from pre-treatment conditioned pain modulation. Such an approach is quite interesting in the context of milnacipran as DNICs are involved in the mechanism of action of both drugs [12,17]. In this trial, we set the mechanistic hypothesis that (1) milnacipran restores the function of descending inhibitory pathways and concomitantly decreases the pain experience in fibromyalgia patients, and (2) this efficacy could be predicted from the performance, before treatment, of pain descending pathways when activated by conditioned pain modulation.

Methods/design

This study is a prospective, randomized, controlled, double blind clinical trial of two parallel groups, milnacipran versus placebo, in 48 fibromyalgia patients. It is carried out in the Pain Clinic and Clinical Pharmacology Center, University Hospital, Clermont-Ferrand, France. The research ethics committee (Comité de Protection des Personnes Sud-Est 6) gave its approval on October, 18, 2012 (institutional review board number 00008526/AU987), and the Agence Nationale de Sécurité du Médicament et des Produits de Santé on September, 25, 2012, and this trial is registered in ClinicalTrials.gov (trial number NCT01747044).

Patients come twice to the Pain Clinic and Clinical Pharmacology Center, for inclusion and randomization and 1 month later for reassessment.

Eligibility criteria are verified with a complete clinical exam, matching the American College of Rheumatology’s definition of fibromyalgia. Patients meeting the inclusion criteria sign a consent form after receiving oral and written information about the study. At baseline, pain is assessed by a numeric pain rating scale and patients undergo psychophysical and cognitive ability tests. Patients are then randomly assigned to milnacipran (n = 24) or placebo (n = 24) for one month’s treatment, with the following titration: 50 mg on the first three days, 75 mg from day 4 to day 6 and 100 mg from day 7 to 1 month. Evaluations and tests are then repeated 1 month later at visit 2. To maintain good compliance and to verify adverse events, patients are telephoned once a week by a clinical research assistant until visit 2.

Objectives

The primary objective of this trial is to assess whether milnacipran has an influence on DNIC status, by measuring if there is a difference between the results of the conditioned pain modulation test in milnacipran and placebo groups.

The secondary objectives are to assess:

  • Whether the DNIC status could be predictive of milnacipran efficacy in fibromyalgia,

  • The evolution of pain threshold with milnacipran,

  • The impact of milnacipran on cognitive parameters; comprehension tests, executive function, memory, attention and decision making,

  • Tolerance towards milnacipran.

Participants and setting

Inclusion criteria

Patients are eligible for this study if they are over 18 years old with a confirmed diagnosis of fibromyalgia, are able to understand and willing to follow the study protocol and have given informed consent.

Exclusion criteria

Patients will not be accepted if there is contra-indication of milnacipran treatment, if they have hypertension or heart disease, known renal impairment, a medical or surgical history incompatible with the study, or a psychiatric disorder, or if they have shown signs of suicidal behavior or significant suicidal ideas. This study also excludes patients with diabetes, patients with acute and chronic intoxication with alcohol, hypnotics, analgesics, or opioids, patients taking diuretics or a treatment inducing hyponatremia, patients taking non-steroidal anti-inflammatory drugs, oral anticoagulants, aspirin or other drugs that are likely to induce bleeding, and patients taking drugs with serotonin and noradrenaline reuptake inhibition, digitalis, cytochrome P450 1A2 inhibitors, or 5-hydroxytryptamine serotonin receptor agonist. Women of childbearing age not using an effective contraceptive will be excluded, as will pregnant or breastfeeding women, patients taking part in another interventional trial or patients unable to understand the patient information and the informed consent form.

Eligibility and randomization

Patients are recruited during their admission to the Pain Clinic and Clinical Pharmacology Center. Before enrolment, informed consent is obtained from each patient in the presence of the investigator. Randomization will be conducted to balance group sizes according to a computer-generated allocation sequence by blocks with Stata software by a statistician independent of the protocol [20]. The randomization sequence is generated using random blocks and the size of the blocks is unknown, to avoid guessing during the trial. Subjects are then randomized to milnacipran or placebo groups. Double blinding will be fully respected with the patients and the members of staff. A research nurse who is only involved in drug allocation will be in charge of drug administration. Treatments are prepared in the Central Pharmacy of the University Hospital with double blinding according to Good Pharmaceutical Practice. The milnacipran and placebo will be administered in the form of white capsules that look alike.

Definition of outcome measures

Primary outcome measure

The primary outcome measure is the change of conditioned pain modulation effect induced by milnacipran compared with placebo.

Secondary outcome measures

Secondary outcome measures are the assessment of the evolution of pain threshold, DNIC status, milnacipran efficacy and tolerance, and cognitive status.

The summary of the different evaluations and tests is reported in Table 1.

Table 1 Summary of evaluation for a patient

Conditioned pain modulation

Conditioned pain modulation is evaluated before treatment randomization (visit 1, CPMv1) and after 1 month treatment (visit 3, CPMv3). The milnacipran and placebo differences (CPMv3 − CPMv1) are then compared. With pain intensity rated by the patient on a numeric scale from 0 (no pain) to 100 (worst pain possible), the conditioned pain modulation is obtained with the following experiment. An Advanced Thermal Stimulator thermode (Medoc Ltd, Ramat Yishai, Israel) is applied to the volar side of the patient’s dominant forearm. The Medoc PATHWAY system delivers stimulation at the predetermined pain threshold for 10 seconds and the patient rates her pain using the numeric scale. Then the Medoc PATHWAY system delivers a stimulus at the same temperature for 30 seconds and the patient rates her pain using the numerical scale. After the end of these two stimuli (15 minutes), the patient puts the non-dominant hand into a water bath at 46.5°C for 60 seconds. After having dried her hand, the patient has a similar sequence of stimuli for 10 and 30 seconds with pain evaluation using the numeric pain rating scale. The aim of this test is to trigger the stimulation of pain descending pathways. If these pathways are functional, the second series of stimuli will be less painful than the first one because of the inhibitory effect on pain stimuli. It is the reverse if these pathways are not functional, as described in a number of chronic pain situations including fibromyalgia [11,21]. The amplitude of the conditioned pain modulation is given by the difference between the pain scores on the numeric pain rating scale before and after the immersion of the non-dominant hand.

Assessment of pain thresholds with a thermal stimulus

The Advanced Thermal Stimulator thermode (30 × 30 mm) connected to the Medoc PATHWAY system is applied to the volar side of the patient’s dominant forearm. From the baseline value of 32°C, the Medoc PATHWAY system delivers an adjustable temperature peak (in cold and heat, depending on a regular increase of 1°C increments) and is controlled by rapid feedback. This device is used to evaluate the pain threshold to heat and cold by calculating the mean of three measures. This technique was recently used successfully in neurophysiology studies in human beings [11] and showed similar results to those obtained with a laser [22].

Test-stimulus intensity ‘pain 60/stimulus’

The Advanced Thermal Stimulator thermode is applied to the volar side of the patient’s dominant forearm. From the baseline value of 32°C, the PATHWAY system delivers a series of peaks starting at 1°C above the pain threshold. Then the temperature increases by 1°C until the patient rates the pain intensity as equivalent to 6/10 on the numeric pain rating scale.

Cognitive tests

The Cambridge Neuropsychological Test Automated Battery (Cantab®, Cambridge, UK) [19] is a battery of 22 neuropsychological tests, administered to subjects using a touch screen computer and a press-pad. The tests selected are: Motor Screening Test, Stockings of Cambridge, Reaction Time, Cambridge Gambling Task, and Graded Naming Test.

Data handling and record keeping

All original records, such as consent forms and case report forms, will be archived at the trial site for 15 years. The database file will be anonymized and will also be maintained for 15 years.

Sample size calculation

According to our previous work and a study of the literature [13], we calculate that a sample size of n = 24 patients per randomized group would provide 90% statistical power of detecting an absolute difference of 15 points in the primary outcome, that is, the conditioned pain modulation difference between milnacipran and placebo (with a standard deviation of conditioned pain modulation variation equal to 16 points), at a two-sided alpha level of 0.05. A total of 48 patients will be included.

Statistical analysis

Statistical analysis will be conducted on an intention-to-treat principle using Stata software, version 13 (StataCorp, College Station, TX, USA). A two-sided P value of less than 0.05 will be considered to indicate statistical significance. Baseline characteristics will be presented for each randomized group as the mean ± standard deviation or the median (interquartile range) according to statistical distribution for continuous data, and as the number of patients and associated percentages for categorical parameters. Comparisons between independent groups will be analyzed using the Chi squared or Fisher’s exact test for categorical variables, and by Student’s t-test or the Mann–Whitney test for quantitative parameters (notably primary outcome, temporal summation, test-stimulus intensity ‘pain 60/stimulus’, pain rating on the numeric pain rating scale, cognitive parameters, with normality verified by the Shapiro-Wilk test and homoscedasticity by the Fisher-Snedecor test. As suggested by Vickers and Altman [23], the primary analysis will be completed by an analysis of covariance considering conditioned pain modulation at 1 month as a dependent variable, and group and baseline value of conditioned pain modulation as independent parameters. Finally, to study whether the DNICs (assessed using the conditioned pain modulation test) in patients with fibromyalgia would be predictive of milnacipran efficacy, multivariate models such as regression analysis (milnacipran efficacy evaluated by conditioned pain modulation difference taken as a dependant variable [13]) will be performed considering the randomization group and the baseline values of conditioned pain modulation and pain as covariables. Secondarily, a sensitivity analysis concerning missing data will be considered to study their nature (not missing at randomization, missing at randomization and so on) and to propose the most appropriate imputation approach.

Discussion

Evaluation of predictive factors of pain development and pain alleviation is very important for treatment optimization [24]. Pain alleviation in fibromyalgia is very difficult, as the response to analgesics is very variable. Milnacipran is particularly recommended for the management of fibromyalgia [16] but only 40% of patients are relieved (30% less pain) [18]. Adding to this high variability in the response to milnacipran, discontinuation of treatment is also due to adverse events in 25% of patients compared with 12% in those receiving placebo [25]. Considering that many patients have no improvement of pain symptoms, it is therefore important to explore the status of the pain modulatory system and evaluate whether DNICs could be a predictive factor of the efficacy of milnacipran in patients with fibromyalgia. The comparison of the performance of descending inhibitory pathways when triggered by a painful stimulus before and after treatment gives information on the amplitude of pain modulation and control. It may help to predict non-responders, as shown for duloxetine [13], and identify the risk of developing chronic post-operative pain [26]. This study aims first to evaluate the state of functioning of the DNICs in patients with fibromyalgia and then to estimate if it might be a predictive factor of pain alleviation. If such an impact is demonstrated, clinicians could perform a simple psychophysical test to test the DNIC performance before prescribing milnacipran. Considering the tight links between chronic pain and cognitive impairment [19], the study will also assess the impact of milnacipran on several cognition domains. This approach could help to optimize treatment, would avoid useless prescription, prevent unnecessary adverse events, and, more generally, would prevent recurrent therapeutic failure in non-responder patients.

Trial status

Recruitment started in April 2013. At the time of writing, 26 patients had been recruited.

Abbreviations

CPMv1:

conditioned pain modulation test, visit 1

CPMv3:

conditioned pain modulation test, visit 3

DNIC:

diffuse noxious inhibitory control

References

  1. Bannwarth B, Blotman F, Roué-Le Lay K, Caubère J-P, André E, Taïeb C. Fibromyalgia syndrome in the general population of France: a prevalence study. Joint Bone Spine. 2009;76:184–7.

    Article  PubMed  Google Scholar 

  2. Mease P. Fibromyalgia syndrome: review of clinical presentation, pathogenesis, outcome measures, and treatment. J Rheumatol Suppl. 2005;75:6–21.

    PubMed  Google Scholar 

  3. Branco JC, Cherin P, Montagne A, Bouroubi A. Multinational coordinator study group. Longterm therapeutic response to milnacipran treatment for fibromyalgia: a European 1-year extension study following a 3-month study. J Rheumatol. 2011;38:1403–12.

    Article  CAS  PubMed  Google Scholar 

  4. Wolfe F, Clauw DJ, Fitzcharles M-A, Goldenberg DL, Katz RS, Mease P, et al. The American College of Rheumatology preliminary diagnostic criteria for fibromyalgia and measurement of symptom severity. Arthritis Care Res. 2010;62:600–10.

    Article  Google Scholar 

  5. Kosek E, Hansson P. Modulatory influence on somatosensory perception from vibration and heterotopic noxious conditioning stimulation (HNCS) in fibromyalgia patients and healthy subjects. Pain. 1997;70:41–51.

    Article  CAS  PubMed  Google Scholar 

  6. Lautenbacher S, Rollman GB. Possible deficiencies of pain modulation in fibromyalgia. Clin J Pain. 1997;13:189–96.

    Article  CAS  PubMed  Google Scholar 

  7. Sigurdsson A, Maixner W. Effects of experimental and clinical noxious counterirritants on pain perception. Pain. 1994;57:265–75.

    Article  CAS  PubMed  Google Scholar 

  8. Edwards RR, Ness TJ, Weigent DA, Fillingim RB. Individual differences in diffuse noxious inhibitory controls (DNIC): association with clinical variables. Pain. 2003;106:427–37.

    Article  PubMed  Google Scholar 

  9. Staud R, Robinson ME, Vierck Jr CJ, Price DD. Diffuse noxious inhibitory controls (DNIC) attenuate temporal summation of second pain in normal males but not in normal females or fibromyalgia patients. Pain. 2003;101:167–74.

    Article  PubMed  Google Scholar 

  10. Van Wijk G, Veldhuijzen DS. Perspective on diffuse noxious inhibitory controls as a model of endogenous pain modulation in clinical pain syndromes. J Pain. 2010;11:408–19.

    Article  PubMed  Google Scholar 

  11. Pickering G, Pereira B, Dufour E, Soule S, Dubray C. Impaired modulation of pain in patients with postherpetic neuralgia. Pain Res Manag. 2014;19:e19–23.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Yarnitsky D, Arendt-Nielsen L, Bouhassira D, Edwards RR, Fillingim RB, Granot M, et al. Recommendations on terminology and practice of psychophysical DNIC testing. Eur J Pain. 2010;14:339.

    Article  PubMed  Google Scholar 

  13. Yarnitsky D, Granot M, Nahman-Averbuch H, Khamaisi M, Granovsky Y. Conditioned pain modulation predicts duloxetine efficacy in painful diabetic neuropathy. Pain. 2012;153:1193–8.

    Article  CAS  PubMed  Google Scholar 

  14. Carville SF, Arendt-Nielsen S, Bliddal H, Blotman F, Branco JC, Buskila D, et al. EULAR evidence-based recommendations for the management of fibromyalgia syndrome. Ann Rheum Dis. 2008;67:536–41.

    Article  CAS  PubMed  Google Scholar 

  15. Russell IJ, Mease PJ, Smith TR, Kajdasz DK, Wohlreich MM, Detke MJ, et al. Efficacy and safety of duloxetine for treatment of fibromyalgia in patients with or without major depressive disorder: results from a 6-month, randomized, double-blind, placebo-controlled, fixed-dose trial. Pain. 2008;136:432–44.

    Article  CAS  PubMed  Google Scholar 

  16. Ormseth MJ, Eyler AE, Hammonds CL, Boomershine CS. Milnacipran for the management of fibromyalgia syndrome. J Pain Res. 2010;3:15–24.

    CAS  PubMed  PubMed Central  Google Scholar 

  17. Palmer RH, Periclou A, Banerjee P. Milnacipran: a selective serotonin and norepinephrine dual reuptake inhibitor for the management of fibromyalgia. Ther Adv Musculoskelet Dis. 2010;2:201–20.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Arnold LM, Palmer RH, Ma Y. A 3-year, open-label, flexible-dosing study of milnacipran for the treatment of fibromyalgia. Clin J Pain. 2013;29:1021–8.

    Article  PubMed  Google Scholar 

  19. Pickering G, Pereira B, Clère F, Sorel M, de Montgazon G, Navez M, et al. Cognitive function in older patients with postherpetic neuralgia. Pain Pract Off J World Inst Pain. 2014;14:E1–7.

    Article  Google Scholar 

  20. Efird J. Blocked randomization with randomly selected block sizes. Int J Environ Res Public Health. 2011;8(1):15–20.

    Article  PubMed  Google Scholar 

  21. Julien N, Goffaux P, Arsenault P, Marchand S. Widespread pain in fibromyalgia is related to a deficit of endogenous pain inhibition. Pain. 2005;114(1–2):295–302.

    Article  PubMed  Google Scholar 

  22. Granovsky Y, Matre D, Sokolik A, Lorenz J, Casey KL. Thermoreceptive innervation of human glabrous and hairy skin: a contact heat evoked potential analysis. Pain. 2005;115:238–47.

    Article  PubMed  Google Scholar 

  23. Vickers AJ, Altman DG. Statistics notes: analysing controlled trials with baseline and follow up measurements. BMJ. 2001;323(7321):1123–4.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Denk F, McMahon SB, Tracey I. Pain vulnerability: a neurobiological perspective. Nat Neurosci. 2014;17:192–200.

    Article  CAS  PubMed  Google Scholar 

  25. Gendreau J, Palmer R, Thacker K. (170) Milnacipran is safe and well tolerated in the treatment of fibromyalgia syndrome. J Pain. 2008;9(4, suppl, 2):18–8.

    Article  Google Scholar 

  26. Yarnitsky D, Crispel Y, Eisenberg E, Granovsky Y, Ben-Nun A, Sprecher E, et al. Prediction of chronic post-operative pain: pre-operative DNIC testing identifies patients at risk. Pain. 2008;138:22–8.

    Article  PubMed  Google Scholar 

Download references

Funding

This study received a grant from the APICIL foundation in March 2014.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Gisèle Pickering.

Additional information

Competing interests

The authors declare that there are no financial or non-financial competing interests, neither within the conception nor within the conduction of the trial.

Authors’ contributions

GP is the overall study principal investigator; she participated in the conception and study design and contributed to the writing of the study protocol and the drafting and editing of this manuscript. NM, CS, CD, and BP all participated in the study design. BP, NM, and CD contributed to the writing of the study protocol. BP carried out all statistical calculations and wrote the section on statistical analysis in the study protocol. He contributed with GP, CS, and NM to the drafting and editing of this manuscript and the interpretation of data for the work. All authors read and approved the final manuscript.

Rights and permissions

Open Access  This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made.

The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.

To view a copy of this licence, visit https://creativecommons.org/licenses/by/4.0/.

The Creative Commons Public Domain Dedication waiver (https://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Macian, N., Pereira, B., Shinjo, C. et al. Fibromyalgia, milnacipran and experimental pain modulation: study protocol for a double blind randomized controlled trial. Trials 16, 134 (2015). https://doi.org/10.1186/s13063-015-0659-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13063-015-0659-4

Keywords