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Acupuncture lowering blood pressure for secondary prevention of stroke: a study protocol for a multicenter randomized controlled trial



Stroke is the prime cause of morbidity and mortality in the general population, and hypertension will increase the recurrence and mortality of stroke. We report a protocol of a pragmatic randomized controlled trial (RCT) using blood pressure (BP)-lowering acupuncture add-on treatment to treat patients with hypertension and stroke.


This is a large-scale, multicenter, subject-, assessor- and analyst-blinded, pragmatic RCT. A total of 480 patients with hypertension and ischemic stroke will be randomly assigned to two groups: an experimental group and a control group. The experimental group will receive “HuoXueSanFeng” acupuncture combined with one antihypertensive medication in addition to routine ischemic stroke treatment. The control group will only receive one antihypertensive medication and basic treatments for ischemic stroke. HuoXueSanFeng acupuncture will be given for six sessions weekly for the first 6 weeks and three times weekly for the next 6 weeks. A 9-month follow-up will, thereafter, be conducted. Antihypertensive medication will be adjusted based on BP levels. The primary outcome will be the recurrence of stroke. The secondary outcomes including 24-h ambulatory BP, the TCM syndrome score, the Short Form 36-item Health Survey (SF-36), the National Institute of Health Stroke Scale (NIHSS), as well as the Barthel Index (BI) scale will be assessed at baseline, 6 weeks and 12 weeks post initiating treatments; cardiac ultrasound, carotid artery ultrasound, transcranial Doppler, and lower extremity ultrasound will be evaluated at baseline and 12 weeks after treatment. The safety of acupuncture will also be assessed.


We aim to determine the clinical effects of controlling BP for secondary prevention of stroke with acupuncture add-on treatment.

Trial registration, ID: NCT02967484. Registered on 13 February 2017; last updated on 27 June 2017.

Peer Review reports


Worldwide, stroke is a leading cause of death and disability [1,2,3]. A patient with a history of stroke is more vulnerable to recurrence [4, 5]. Especially in China, the recurrence rate of stroke is higher than that of western countries [6, 7]. Recurrent stroke demonstrates higher mortality and disability rates than the previous stroke, which is a heavy burden on both health care resources and society in general [7, 8]. Ischemic stroke is the most common type of stroke and 72.7% of Chinese ischemic stroke patients also suffer from hypertension [6], an independent risk factor for stroke recurrence [9]. Therefore, it would be of great benefit in combating stroke recurrence to decrease blood pressure (BP).

Antihypertensive medications have been regularly used to reduce BP; however, low adherence to antihypertensive medications is prevalent due to various factors including prior experience of medication side effects [10], leading to poor BP control [11]. Uncontrolled BP maybe related to side effects or interactions of antihypertensives and this observation is more commonly noted in older populations [12, 13]. Moreover, a former meta-analysis has shown that only angiotensin-converting enzyme inhibition (ACEI) plus diuretics significantly decreases recurrent stroke events, and no significant association between BP reduction and all adverse outcomes was found [14]. It is apparent that the benefit of ACEI plus diuretics for secondary prevention of stroke is explained by mechanisms beyond the effects of lowering BP alone. The underlying mechanisms may be the divergent cardiovascular effects of ACEI [15], and the ability of diuretics to reduce proteinuria and protect the vascular endothelium [16]. Additionally, the presence of a J-shaped relationship between BP and risk of recurrent stroke is, to a certain degree, confirmed by previous research [17]. Under this context, in order to effectively regulate BP for reducing stroke recurrence, it is urgent to find an alternative that will affect multiple targets.

Acupuncture, with a long history of development in Chinese medicine, is becoming the focus of clinical researchers as an alternative for treating hypertension [18, 19]. Acupuncture-induced regulation of BP has been found to involve peripheral and central neural systems [20] and immune modulation mechanisms [21]. Its multiple-target features might explain the potential of acupuncture in effectively regulating BP to reduce stroke recurrence.

The synergistic BP-lowering effectiveness of acupuncture and antihypertensive agents has been proven, despite there formerly being insufficient evidence for acupuncture alone in lowering BP [22]. Recently, researchers have reported some positive results regarding sole acupuncture treatment for hypertension [23,24,25]. The reasons for this paradoxical situation could be disparities in acupuncture manipulation skills as well as other technical factors. Considering the limited reporting quality, the effect of pure acupuncture in lowering BP remains elusive.

Given that complementary and alternative interventions are recommended for mild and moderate hypertensive patients [26], we cautiously decided to select the hypertensive patients with uncontrolled BP (systolic BP ≥ 140 and < 160, or/and diastolic BP ≥ 90 and < 100 mmHg) who were taking one class of antihypertensive drugs to be the participants. The difference between the control and experimental groups is that in our experimental group, after a period of BP-lowering acupuncture add-on treatment, i.e., the “HuoXueSanFeng” needling method which has been proved to positively treat primary hypertension [27,28,29,30,31,32,33], if the BP falls below 140/90 mmHg, the prior antihypertensive drugs will be ceased, so as to observe the clinical effects of pure acupuncture on BP. Moreover, aiming to create a situation that is analogous to the real world, antihypertensive drugs will be adjusted based on the patients’ BP readings (detailed in the “Antihypertensive medication adjustment” section below) in both groups, respectively.

Altogether, our team conceived this high-quality, pragmatic randomized controlled clinical trial with the primary objective to determine whether BP-lowering acupuncture add-on therapy could decrease the recurrence of first-time ischemic stroke in patients during the 9-month follow-up period.


Study design and setting

Our study is a prospective, multicenter, subject-, assessor-, and analyst-blinded, pragmatic randomized controlled trial. The research period lasts from May 2015 to May 2020 (201507001-08). Five centers from five cities will be involved in recruitments, treatments, and assessments. Informed consent will be obtained after screening for eligibility, then baseline assessments will be conducted before randomization (details in Table 1). Eligible patients will be allocated, in a 1:1 ratio using a dynamic randomization procedure, into a BP-lowering acupuncture therapy group (experimental group) and a control group. After randomization, the patients in the experimental group will be additionally treated by the HuoXueSanFeng needling method (a BP-lowering regimen) plus the “XingNaoKaiQiao” needling method [34] (a formula for stroke) over 12 weeks, whereas the control group will be only given the XingNaoKaiQiao needling method for 12 weeks. Other routine ischemic stroke treatments in both groups will be provided. During the whole process of our study, the antihypertensive medications will be adjusted based on the BP level in the two groups (details displayed in the “Antihypertensive medication adjustment” section). The primary outcome will be all recurrent stroke cases over a follow-up period of 9 months after receiving 12-week acupuncture treatments. Our protocol presentation is in accordance with the Standard Protocol Items: Recommendations for Interventional Trials 2013 (SPIRIT 2013) guidelines. The study flowchart is presented as Fig. 1.

Table 1 Study schedule
Fig. 1
figure 1

Study flowchart®: XingNaoKaiQiao acupuncture + other routine ischemic stroke interventions + one class of antihypertensive drug. ABPM ambulatory blood pressure monitoring, NIHSS National Institute of Health stroke scale, BI Barthel Index, ESRS Essen Stroke Risk Score, TCM traditional Chinese medicine, SF-36 the medical outcome study (MOS) 36-item Short Form Health Survey, NO nitric oxide, ET endothelin, Hcy homocysteine, sCD40L soluble CD40 ligand, ECG electrocardiogram


We will recruit 480 eligible patients from (1) The First Teaching Hospital of Tianjin University of traditional Chinese medicine (TCM), (2) Longhua Hospital Shanghai University of Traditional Chinese Medicine, (3) Chongqing Traditional Chinese Medicine Hospital, (4) Mianyang Hospital of Traditional Chinese Medicine, and (5) Shenzhen Bao’An Traditional Chinese Medicine Hospital Group. The eligible patients must satisfy the criteria defined below. Patients who express a general interest in taking part in the study will meet with one of the study personnel to be informed of all necessary information in oral and written form. After fulfilling the criteria and signing the consent, the study personnel will assign the patient to the acupuncturist and the neurologist who is in charge of the patient.

Inclusion criteria

Patients will be further screened for eligibility if they fulfill all of the following inclusion criteria: (1) first-ever ischemic stroke that has been confirmed by cranial computed tomography (CT) or magnetic resonance imaging (MRI), with stroke duration over 2 weeks and less than 6 weeks; (2) BP below 160/100 mmHg on using one antihypertensive medication except the fixed-dose combinations, for at least 2 weeks; (3) aged 35 to 70 years; and (4) voluntary informed consent signed.

Exclusion criteria

Patients will be excluded if they have any one of the following: (1) secondary hypertension, (2) antihypertensive medication general use for reasons other than BP control, such as long-term need for beta-blockers or diuretics or non-dihydropyridine calcium channel antagonists for cardiac conditions, (3) BP below 140/90 mmHg when taking one hypotensive drug, (4) other coexisting nervous system diseases like epilepsy and peripheral nerve injuries, (5) severe hematopoietic system conditions, coagulation dysfunction, and cancers, (6) diabetic nephropathy, severe liver and renal function impairment, severe heart or lung dysfunction, and arrhythmia, (7) local infection at or around the acupoint, (8) pregnant or lactating women, and (9) recruitment into other clinical trials within 1 month.

Ethical issues

Our protocol complies with the principles of the Declaration of Helsinki and has been approved by the central Independent Ethics Committee (IEC) of The First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine (TCM) for the various centers (reference number: TYLL2016[K]NO.007). We have also registered at (NCT02967484). The overall supervision of our trial will be in the charge of the central IEC of the First Affiliated Hospital of Tianjin University of TCM; any change in the protocol will be submitted to, and decided by, the Ethics Committee.

Recruitment strategies

Firstly, all the patients will be enrolled from the inpatient departments of the acupuncture and moxibustion sections of each branch center, to fulfill the completion of the consistent acupuncture treatments for 6 weeks. We will also use advertisements, such as printed recruitment posters, in each participating hospital, and the various social media platforms to distribute the trial information.

Informed consent

The details of our study, including trial objectives, characteristics, probable benefits and risks, other available treatment alternatives, and the subjects’ rights as well as obligations as stated in the Declaration of Helsinki, will be made clear to the patients by a study personnel who has their grouping code, and their agreement will be required. After obtaining the written informed consent, the subjects will be enrolled in the study.

During the process of the trial, if new points regarding the study ethics emerge, written revisions regarding the informed consent will be handled by the Ethics Committee and, after their approval, the individuals’ consent will be requested again. In case of the patients’ withdrawal, their available data will be kept for the final analyses.

Randomization and allocation concealment

All the eligible participants will be randomized into the experimental group or the control group, in a 1:1 ratio, using minimization, a dynamic random allocation technique by the MINIM program installed in each separate center. The baseline prognostic factors related to stroke recurrence, including age, categorized as 35–50, 51–65, and 66–70 years), gender, smoking status, diabetic status and atrial fibrillation, classified as “no” or “yes with/without anti-coagulation,” will be balanced between groups according to the minimization procedures. The computer-generated randomization grouping code will be offered after the recruitment of the eligible patients so that allocation concealment should be ensured.

Interventions (Table 2)

Table 2 Protocol form

Both groups receiving acupuncture treatments ensures the blinding of subjects.

Experimental group

Patients in the experimental group will be given HuoXueSanFeng acupuncture therapy, in addition to the control group interventions. To ensure the optimal effects of acupuncture stimulation, all the therapists are required to have clinical experience of acupuncture treatments for at least 8 years.

Disposable, sterile needles with a diameter of 0.25 mm and a body length of 40 mm (HUATO, Suzhou, China) will be used. Patients are asked to adopt the supine position. Acupoints used here are bilateral Renying (ST9), Hegu (LI4), Quchi (LI11), Taichong (LR3), and Zusanli (ST36). The acupoint locations with reference to the World Health Organization (WHO) standards in the Western Pacific Region, and the corresponding manipulations of the aforementioned acupoints are listed in Table 3, which accord with those described in a previous paper [32]. All the manipulations will be applied for 1 min and the needles are retained for 30 min.

Table 3 Acupoint form

The patients will be provided with HuoXueSanFeng acupuncture treatments six times per week in the first 6 weeks, referred to as the consistent treatment period. The consolidation period consists of three sessions of HuoXueSanFeng acupuncture treatments weekly in the following 6 weeks with a total of 12 weeks of HuoXueSanFeng acupuncture treatments performed in the experimental group.

Control group

The control group will receive one antihypertensive medication on the basis of ischemic stroke routine care. In our trial, basic ischemic stroke medical care includes 12 weeks of XingNaoKaiQiao needling therapy plus other forms of routine stroke care. Twelve weeks of XingNaoKaiQiao needling therapy should also aid in the improvement of compliance in both groups for its high acceptance and remarkable effectiveness for stroke. All medications must be recorded in the drug combination form, including the types, dosage, usage frequency and time, etc., in order to provide data for analysis and the report summary. The acupuncture needle is the same with that used in HuoXueSanFeng acupuncture treatments. The acupoint locations and manipulations are presented in Table 3. No common acupoints are used in the two formulas. The retention time and frequency of treatments are identical to HuoXueSanFeng acupuncture therapy. During the entire process of our study, the control-group patients are prohibited from receiving any BP-lowering acupuncture therapy, and any violations will be recorded.

Antihypertensive medication adjustment

After randomization, an electronic BP machine and a BP diary notebook will be delivered to all patients for measuring and recording their BP levels. During the first 6-week inpatient treatments, they will be instructed how to use the machine accurately. BP will be measured within 1 h after morning waking before taking antihypertensive medications, at 3 h after taking antihypertensive medications, at 4 p.m. and before bedtime over the entire process. On each occasion, three repeated measurements of supine BP, following a rest of at least 15 min, will be conducted at 1-min intervals. The antihypertensive medication classes in both groups will be recorded. Lifestyle advice regarding hypertension and stroke will be given to the patients. In the experimental group, if the patients have a mean BP level below 140/90 mmHg for three consistent days, they will receive solely acupuncture treatment; thereafter, once their BP levels increase to ≥ 140 mmHg systolic and/or ≥ 90 mmHg diastolic for 1 month, prior antihypertensive medications should be re-dispensed. Otherwise, if BP levels are ≥ 160 mmHg systolic and/or ≥ 100 mmHg diastolic for three consistent days after initiating HuoXueSanFeng acupuncture treatments or over the follow-up period, additional antihypertensives should be prescribed. All the medication adjustments will be filled out in the Case Report Forms (CRFs).

For the control group, when the average systolic BP increases to ≥ 160 mmHg and/or diastolic BP ≥ 100 mmHg lasting for three continuous days in the study period, other antihypertensive drugs will be prescribed in the opinion of the treating physicians, and these will be documented for final analyses.

Outcome assessments

The assessors are blinded to grouping. The primary outcome will be all cases of recurrent stroke over a follow-up period of 9 months after receiving 12-week acupuncture treatments. Secondary endpoints, such as 24-h ambulatory BP, TCM syndrome score, Short Form 36-item Health Survey (SF-36) results, National Institute of Health Stroke Scale (NIHSS) and Barthel Index (BI) scale scores will be assessed at baseline, 6 weeks, and 12 weeks post initiating treatments; serum nitric oxide (NO), endothelin (ET), homocysteine (Hcy), soluble CD40 ligand (sCD40L), and copeptin levels and cardiac ultrasound, carotid artery ultrasound, transcranial Doppler, and lower extremity ultrasound results will be evaluated at baseline and 12 weeks after treatment. Other safety indicators including baseline general physical examination, blood, urine, and stool routine tests, coagulation function, D-dimer level, liver and kidney function, electrocardiograph as well as a chest X-ray will also be examined 12 weeks after randomization. At 6 months after randomization, blood, urine, and stool routine tests, coagulation function, D-dimer level, liver and kidney function, electrocardiograph, NO, ET, Hcy, sCD40L, and copeptin tests will be re-checked, with some hope of improving patients’ adherence to treatment. All-cause mortality will also be evaluated during the follow-up period. The Essen Stroke Risk Score (ESRS) will be additionally assessed at baseline and 1 year post randomization.


After finishing the acupuncture treatments, patients will be followed up monthly via telephone for 1 year post randomization. Stroke recurrence, all-cause deaths and BP control will be investigated and recorded in the CRFs. The patients will be required to use the BP diaries to record their BP four times daily. If the BP is ≤ 160 mmHg systolic and/or ≤ 100 mmHg diastolic for 1 month, the patient will be advised to take antihypertensive medications, which will be documented in the CRF.

Sample size and statistical methods

The sample size calculation of the study was based on China’s Ministry of Health data suggesting that at least 197 patients are required in each group for the final analysis to achieve a power of 80% to demonstrate a recurrence rate of 7%, rather than 16% resulting from HuoXueSanFeng acupuncture (data not shown, please see Additional file 1), at a two-sided significance level of 5%. Given a projected dropout rate of 15%, we aimed to recruit 480 patients for the study.

Statistical analysis will be conducted by a third party who is unaware of the treatment allocation. Data will be analyzed with SAS 9.1 and SPSS 19.0 software packages. Two-sided P < 0.05 represents statistical significance for all the analyses. Both intention-to-treat analysis (ITT) and per-protocol (PP) analysis will be performed. We will compare the result of ITT analysis with that of PP analysis to determine whether the results are consistent. For the ITT analysis, missing data will be handled by Last Observation Carry Forward rules, in brief, the finally observed data will be used for replacement of the missing primary variables.

Baseline demographic characteristics, including individual variables, such as age, sex, history of atrial fibrillation with or without current anti-coagulation medication, history of diabetes and smoking, and other baseline values, will be expressed with descriptive statistics for the two groups. For the primary outcome, recurrent stroke events, and secondary outcomes, the mortality rate and detailed causes (stroke or non-stroke), will be described as percentage (%), between-group difference will be analyzed using the chi-square test or Fisher’s exact test. For filling in the daily BP diary, it is required to measure BP four times each day at baseline before treatment, 2 weeks, 6 weeks, 12 weeks, 6 months, and 1 year after treatment. We will compare between-group or within-group values at the indicated time points. For highly effective use of the daily BP data, on one hand, we will collect all the values of the measurements at the same time in the day until each predesigned time point for comparison and, on the other hand, we will collate the four daily measurements to yield an average value in a day for later comparison at the time points mentioned above. Other secondary endpoints at different time points will also be compared. All the above different time-point assessments will be analyzed by repeated measures analysis of variance (ANOVA). Adverse events in each group will be documented as percentage (%) for safety assessments using the chi-square test or Fisher’s exact test.

Patient safety

In the process of acupuncture treatment, possible adverse events (AEs) including subcutaneous hematoma, infection, alcohol allergy, etc., will be observed in detail and documented in the CRFs. Causality between acupuncture and AEs will be assessed. If serious AEs do occur, the grouping will be un-blinded and we will report the AE to the project leader (PL) and Ethics Committee immediately, who will make a decision on whether the participant needs to be withdrawn from the study, or whether the trial should be adjusted or terminated. For those who suffer harm from trial participation, we will treat them free of charge until they recover.

Data management and quality control

The teaching and research office of epidemiology and statistics of the Chinese People’s Armed Police Force Logistics College is fully responsible for the data management of the project. Prior to the project, the center has been involved in the design of the project, which has been discussed twice monthly with the principle experts in the State Administration of Traditional Chinese Medicine of the People’s Republic of China, and project implementation throughout the process has successfully completed quality control and data management scrutiny. A specific research assistant (RA), who is masked to treatment allocation, will enter the clinical data. Data will be obtained by direct questions to patients, from medical records, and a the patient’s relative or proxy. The personal information of the patients will be kept in the specific files with pre-set codes. Entering data into CRFs and other essential skills was covered during the training session prior to study commencement.

All the researchers will accept centralized and unified training before research implementation to help them become familiar with, and master, the diagnosis, treatment measures and basic assessment skills, in order to improve the researchers’ internal observation consistency. A three-level inspector appointed for the national Chinese Medicine Clinical Research Base Unit, First Teaching Hospital of Tianjin University of TCM, and each subcenter will regularly carry out quality monitoring and supervision throughout the study.


We plan to publish several Chinese and English articles, and hold one or two seminars yearly to disseminate part of our new findings to health care professionals, the public, and other relevant groups. On the other hand, the participants will be instructed on how to better manage their condition after the results yield useful information. After our trial finishes, we will make an effort to share our findings with the experts from other Chinese medical fields, hoping to benefit them by the drafting of stroke and hypertension guidelines incorporated into the features of TCM.

Biological specimens

The patients’ blood samples for the inpatient routine tests will be collected and analyzed as usual. For testing serum NO and ET concentrations, about 3–5 ml venous blood will be collected; after centrifugation, the remaining serum will be subpacked into frozen tubes, followed by concise labeling, then kept for no more than 6 months in a refrigerator at −80 °C until final analysis by the chemical reagent corporation.


Acupuncture within Chinese medicine has become a visible international brand of China. Both stroke and hypertension are heavy global disease burdens and both have alarmingly high comorbidities [35] which are associated with a poorer prognosis. Antihypertensive medications have been commonly used for preventing stroke recurrence. However, evidence-based medicine data regarding secondary prevention of stroke by antihypertensives is controversial [14, 36]. Therefore, it is of great clinical significance that our study aims to decrease recurrent stroke using acupuncture, in the hope of increasing western knowledge of acupuncture.

As early as in 1983, the WHO recommended non-drug therapy as the preliminary and auxiliary treatment of mild-to-moderate hypertension [26]. With the enhancement of people’s drug safety awareness, the proportion of non-drug therapy in the treatment of hypertension has gradually increased. Acupuncture, with its advantages of convenience, satisfactory effects and few adverse reactions [37], is attracting increasing clinical attention and is also becoming one of the hotly debated topics in the study of alternative medicine worldwide.

The acupuncture method of XingNaoKaiQiao for the treatment of stroke was launched in 1972 by the first, and to date, only Chinese academician of engineering in the acupuncture discipline, Xue-min Shi, who devoted himself to introducing acupuncture to the whole world and developed an international academic team that cooperates with Germany, France, Japan, and Singapore, among other countries. For its internationally substantial contributions, XingNaoKaiQiao needling therapy for stroke has been recognized as another special acupuncture technique in addition to acupuncture anesthesia by foreign health care researchers. Besides the confirmed effects for stroke by our own team, the others also reported its encouraging results for stroke patients [38]. With the great success of XingNaoKaiQiao, academician Xue-min Shi gained deeper insight into secondary stroke prevention, and established another acupuncture treatment for hypertension called HuoXueSanFeng, the BP-lowering acupuncture regimen used in our trial. Our previous researches have shown that this acupuncture method reduces BP for primary hypertension patients, and its immediate and long-term antihypertensive efficacy is significant for either BP-lowering or improving the patients’ clinical symptoms [27,28,29,30,31,32,33]. So, here we also want to investigate the BP-controlling effect of HuoXueSanFeng, especially regarding its sole efficacy, in a larger sample size population. In this study, both XingNaoKaiQiao and HuoXueSanFeng needling therapy are performed over the 12-week treatment period; XingNaoKaiQiao therapy is a general treatment for stroke with a high credibility, its free treatment here will enhance adherence with participation. Additionally, because both groups are needled, subject blinding should be ensured, minimizing the placebo effect of acupuncture.

Of note, in our trial, we cautiously selected three secondary endpoints, namely, Hcy, sCD40L, and copeptin levels, which were closely related to stroke recurrence. Elevated Hcy levels have been reported to be indicative of an increased risk for ischemic strokes and recurrent strokes [39]. sCD40L appears to be an independent predictor for stroke recurrence [40]. Copeptin has been studied to be a predictor of both severity at admission and 1-year stroke recurrence in stroke patients [41]. Assessing the influence of our study treatment on them might be reflective of the effects on stroke recurrence via acupuncture lowering hypertension.

The multicenter approach of our study allows more generalisable interpretation of the results and the usage of standardized, cross-culturally adapted assessment allows comparison and pooling of all study data from different trial centers. Considering methodological and ethical reasons, acupuncture will be delivered to both groups to prevent bias through potential placebo effects. To improve operation and observation consistency, the research sets strict rules that must be followed.

The unavoidable weaknesses of our trial are as follows: (1) the five hospitals are located in different cities, so the standard of acupuncture manipulation will differ between them. Therefore, strict training and supervision will be implemented to ensure unified and consistent operation as far as possible, (2) despite the subject- and assessor-blinding, there are still some patients who will likely know which group they are in; therefore, we would keep the patients separate when receiving treatment to avoid them talking to each other; (3) after completion of the 12-week treatment, a 9-month follow-up will be conducted. This time span means that participant compliance could be a problem. Accordingly, we have designed the BP diary and regular telephone follow-up to try to minimize this.



Ambulatory blood pressure monitoring


Angiotensin-converting enzyme inhibition


Adverse events


Analysis of variance


Barthel Index


Blood pressure


Case Report Forms




Essen Stroke Risk Score






Independent Ethics Committee




National Institute of Health Stroke Scale


Nitric oxide


Project leader




Research assistant


Randomized controlled trial


Soluble CD40 ligand


Short Form 36-item Health Survey

SPIRIT 2013:

Standard Protocol Items: Recommendations for Interventional Trials 2013


Traditional Chinese medicine.


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Our work was supported by the project sponsored by the State Administration of Traditional Chinese Medicine of the People’s Republic of China (grant number: 201507001-08).

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All data generated or analyzed during this study are included in this published article (and its Additional files 1 and 2).

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Authors and Affiliations



YZD conceived the study design and provided the professional advice on the drafting profile. XXG, CTW, and HZZ drafted the manuscript. YL and MHW revised the paper and drew the tables and the figure. Academician XMS participated in the study concept. HPB, WLG, XGM, MTW, and CXH polished the final manuscript. All authors read approved the final manuscript.

Corresponding author

Correspondence to Yu-zheng Du.

Ethics declarations

The central Independent Ethics Committee (IEC) of The First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine (TCM) has approved our study for the various centers (reference number: TYLL2016[K]NO.007), and patient consent was obtained before the randomization.

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The authors declare that they have no competing interests.

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Additional files

Additional file 1:

Sample size calculation process. (DOC 31 kb)

Additional file 2:

SPIRIT 2013 Checklist. (DOC 139 kb)

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Du, Yz., Gao, Xx., Wang, CT. et al. Acupuncture lowering blood pressure for secondary prevention of stroke: a study protocol for a multicenter randomized controlled trial. Trials 18, 428 (2017).

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