Skip to main content
  • Study protocol
  • Open access
  • Published:

Chinese herbal formula Xuefu Zhuyu for primary dysmenorrhea patients (CheruPDYS): a study protocol for a randomized placebo-controlled trial



Epidemiological studies have shown that young women often suffer from primary dysmenorrhea (PD) which is a common cause that affects their routine work and quality of life. Chinese herbal medicine has been widely used for PD in China. A systematic review found that Xuefu Zhuyu (XFZY) has a promising effect on PD management, yet there is a dearth of high-quality evidence in support of this claim. We want to conduct a randomized controlled trial to evaluate the efficacy and safety of XFZY for PD patients.


This is a protocol for a multicenter, randomized, placebo-controlled trial. A total of 248 participants with PD will be recruited at 6 centers and randomized into two groups—a herbal treatment group and a placebo group. The participants will receive either XFZY or placebo, three times per day, for 3 menstrual cycles, with a 12-week follow-up. The primary outcome will be the mean change in pain intensity as measured by VAS, while the change in menstrual pain duration, the change in peak pain intensity as measured by VAS, the Cox Menstrual Symptom Scale (CMSS), quality of life EQ-5D-5L, cumulative painkiller consumption, and health economics will be included as secondary outcomes. Adverse events will also be reported.


This protocol describes a multicenter, double-blind, randomized, placebo-controlled trial that investigates the efficacy and safety of XFZY for primary dysmenorrhea. Validated evaluation tools will assess dysmenorrhea severity. We believe that this research will provide important evidence regarding the use of XFZY to treat dysmenorrhea.

Trial registration

Chinese Clinical Trial Registry ChiCTR1900026819. Registered on 23 October 2019

Peer Review reports


Dysmenorrhea is a common gynecological disease. Its prevalence ranges from 50 to 90% across ethnicities and geographical locations [1]. Dysmenorrhea can be classified into primary dysmenorrhea (PD) and secondary dysmenorrhea, with the former more prevalent in young women [2]. More than one half of PD patients are moderate or severe among Chinese Female University students [3], diminishing young females’ quality of life [3, 4], restricting their daily activities, and causing absenteeism from work and school [3, 4]. Despite its high incidence, most patients do not seek medical help for dysmenorrhea [5].

Non-steroidal anti-inflammatory drugs (NSAIDs) are an effective treatment for PD [5, 6], but can cause adverse events in the gastrointestinal tract and central nervous system [7]. These include indigestion, headaches, and drowsiness [6]. Hormone therapy generally requires periodic, prolonged, or continuous use [5], and patients may find it inconvenient. Therefore, some patients also seek complementary and alternative therapies, including Chinese medicine (CM), to treat PD.

Physicians of Chinese medicine treat patients according to pattern differentiation. Pattern (Zheng or syndrome in Chinese medicine) is a diagnostic conclusion based on pathological changes in a disease at a certain stage. It includes features such as the nature of the disease, cause, location, and development trends [8]. Qi stagnation and blood stasis pattern (QBP) are common PD patterns [9,10,11]. Its features always present as distending pain and stabbing pain [12]. The CHM formula Xuefu Zhuyu (XFZY) has been widely used in clinical in China [13] and was the most frequently used in research focused on blood stasis in Korea [14]. It comes as both an oral liquid and a capsule [15]. XFZY promotes Qi and activates the blood to relieve QBP symptoms [12].

Pharmacological experiments have found that XFZY restrains platelet aggregation induced by adenosine diphosphate, arachidonic acid, and collagen [16]. This has been shown to inhibit thrombogenesis in rats [16, 17] and increase the number of open capillaries [18]. Thus, it can be inferred that XFZY can treat the pathogenesis of QBP.

XFZY was approved by the China Food and Drug Administration (CFDA) in 2002 [19] and has been included in the Chinese pharmacopeia [20]. XFZY’s components include Persicae semen (Taoren), Carthami flos (Honghua), Rehmanniae radix (Dihuang), Angelicae sinensis radix (Danggui), Chuanxiong rhizome (Chuanxiong), Paeoniaeradix rubra (Chishao), Achyranthis bidentatae radix (Niuxi), Platycodonis radix (Jiegeng), Bupleuri radix (Chaihu), Aurantii fructus (Zhiqiao) fried with bran, and Glycyrrhizae radix et rhizome (Gancao).

A recent systematic review [21] revealed that XFZY has a promising effect on PD management. Some trials also found the efficacy of XFZF on PD. For example, a randomized clinical trial (RCT) [22] found that XFZY had a higher cured rate and a lower recurrence rate compared with indomethacin for PD. Some other trials also found XFZY had a better response rate for PD as compared to conventional medication (e.g., diclofenac sodium, ibuprofen) with head-to-head comparison [23,24,25] or add-on design [26, 27]. Another randomized trial found that compared with fenbid solely, XFZY decoction plus fenbid had a better pain intensity relief [28]. But in the review [21], none of the included trials used a placebo as a control or with blinding of participants and personnel. Moreover, most of the previous trials appeared to be of low methodological quality. So far, XFZY’s efficacy lacks evidence from RCTs with rigorous methodology. Thus, we have designed a multicenter, participant- and personnel-blinded, randomized placebo-controlled trial to evaluate the efficacy and safety of XFZY for PD with QBP.



The aim is to evaluate the efficacy and safety of XFZY for PD patients with QBP in Chinese medicine (CM).

Design and setting

This is a multicenter, randomized, placebo-controlled trial. It will be conducted in 6 university hospitals in different Chinese provinces. A flow chart of this trial is provided in Fig. 1. The trial consists of a treatment period of 3 menstrual cycles and a follow-up period of 3 menstrual cycles. After providing written informed consent, eligible patients will be randomized to receive either XFZY or placebo at a ratio of 1:1.

Fig. 1
figure 1

Flow diagram. VAS, visual analog scale; CMSS, Cox Menstrual Symptom Scale; AEs, adverse events

The trial’s design and conduction will adhere to the Declaration of Helsinki and have been approved by the ethics committees at Guangdong Provincial Hospital of Chinese Medicine (No. BF2019-175-01) and each center. The trial was registered at the Chinese Clinical Trial Registry (No. ChiCTR1900026819) on 23 October 2019.


Diagnostic criteria

PD diagnostic criteria

The diagnostic criteria for dysmenorrhea are based on primary dysmenorrhea consensus guidelines (2017) [5]. PD is characterized by crampy, suprapubic pain before or after the onset of menstrual bleeding. Its symptoms peak with maximum bleeding and may persist for 2–3 days. It is often accompanied by diarrhea, nausea and vomiting, fatigue, dizziness, headache, or even syncope and fever. In this RCT, abdominal ultrasound and gynecological examination will be conducted to exclude secondary dysmenorrhea and other causes of menstrual pain.

QBP diagnostic criteria

QBP diagnosis in CM is based on a scale which has been verified with validity and reliability [29]. Table 1 shows the symptoms and signs evaluated with the diagnostic scale.

Table 1 CM syndrome diagnostic scale for QBP [12]

Inclusion criteria

The following are the inclusion criteria:

  1. 1.

    Meet the diagnostic criteria for PD and QBP in CM

  2. 2.

    Aged 18 to 35 years

  3. 3.

    Menstrual cycle (21 to 35) days

  4. 4.

    Pain visual analog scale (VAS) score > 4

  5. 5.

    Signed informed consent

Exclusion criteria

The following are the exclusion criteria:

  1. 1.

    Secondary dysmenorrhea confirmed by gynecological ultrasound or caused by pelvic inflammation, endometriosis, cervix tumor, endometrial polyp, or other ailments

  2. 2.

    Severe primary cardiovascular, liver, kidney, or blood disease; mental illness (schizophrenia, epilepsy, alcoholism, anorexia, and/or a history of serious mental illness and those taking antidepressants, antiserotonin, barbiturates, or psychotropic drugs); or other severe primary diseases

  3. 3.

    Lactating and pregnant women or women who have recently been preparing for pregnancy

  4. 4.

    Allergy to herbal ingredients in the study

  5. 5.

    Participants in other clinical trials

  6. 6.

    Those who have been treated with hormone drugs over the last 3 months

  7. 7.

    Self-Rating Anxiety Scale (SAS) ≥ 60 or Self-Rating Depression Scale (SDS) > 62


Recruitment advertisements will be posted on hospital notice boards and the WeChat (Shenzhen Tencent Computer System Co. Ltd., Guangdong, China) messaging client to recruit potential participants. Outpatient clinical staff will also screen and refer potential patients who will then access the study information. Interested PD patients can register for this trial by contacting researchers. Researchers will then arrange screening visits with potential participants 0–14 days before their onset of the next menstruation. Participants with PD will be enrolled at one of the following 6 hospitals in 4 different Chinese provinces: (1) Affiliated Hospital of Liaoning University of Traditional Chinese Medicine in Liaoning Province, (2) Guangdong Provincial Hospital of Chinese Medicine in Guangdong Province, (3) The Second Affiliated Hospital of Liaoning University of Traditional Chinese Medicine in Liaoning Province, (4) The First Affiliated Hospital of Heilongjiang University of Chinese Medicine in Heilongjiang Province, (5) The First Hospital of China Medical University in Liaoning Province, and (6) Affiliated Hospital of Inner Mongolia University for the Nationalities in Inner Mongolia Province. A signed consent form will be obtained from every participant who is eligible and willing to participate in the trial.

Randomization and allocation concealment

A center-stratified and permuted block randomization sequence will be generated by SAS 9.2 (SAS Institute Inc., Cary, USA) and performed by the Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences (IBRCM). Eligible participants will be randomly allocated to either the XFZY group or the placebo group at a ratio of 1:1 through the Interactive Web Response System, developed by IBRCM. The randomization sequence will be strictly confidential and maintained by IBRCM. All participants, investigators, outcome assessors, statisticians, and other staff involved in this trial will have no chance to know the treatment allocation until the end of the study.


All participants, investigators, statisticians, pharmacists, and other staff will be blinded to the treatment assignments throughout the trial. The placebo will be identical to the XFZY in appearance, weight, taste, smell, and packaging. When serious adverse events (SAEs)/adverse reactions (SARs) occur or a subject’s condition deteriorates, and it is necessary to know their specific treatment so as to take emergency rescue, then blinding will be uncovered and participants and/or investigators will know the specific treatment. The reason, date, and results of the unblinding will be recorded in a case report form (CRF).


Experimental group

Participants in the experimental group will take XFZY orally three times per day (20 ml each dose) for 14 days before the onset of menstruation. The treatment period will last 3 menstrual cycles (XFZY will be administered for 14 days during each menstrual cycle). After treatment, there will be a 12-week follow-up.

The XFZY will be manufactured by Jilin Aodong Yanbian Pharmaceutical Co. Ltd. (Jilin Province, China) according to the requirements of the Good Manufacturing Practice (GMP). XFZY is composed of 11 herbs: peach kernel, safflower, Rehmannia glutinosa, ligusticum chuanxiong, red peony root, radix platycodonis, radix platycodonis, radix bupleurum, bran fried fructus aurantii, licorice, and Angelica sinensis.

Control group

Patients in the control group will receive a placebo with no active ingredients, but consistent with XFZY in terms of dosage, appearance, smell, taste, and texture. It will also meet the hygiene inspection requirements. The placebo’s primary ingredients are honey, white granulated sugar, fried brown sugar, bitterants, ginseng essence, natural edible pigments, and food antiseptic. The placebo will also be taken orally (20 ml each dose) three times per day for 14 days before the onset of menstruation for 3 menstrual cycles. The placebo is also manufactured by Jilin Aodong Yanbian Pharmaceutical Co. Ltd. in line with the GMP requirements.

Both XFZY and the placebo will be labeled and packaged based on a randomization sequence by Jilin Aodong Yanbian Pharmaceutical Co. Ltd. under the supervision of IBRCM.

A box containing a 14-day dose of either XFZY or placebo will be distributed to subjects in the pharmacy department or clinic office every menstrual cycle, from visit 1 (menstrual cycle 1) to visit 4 (menstrual cycle 4).

Discontinuing interventions

Participants will be free to withdraw from this clinical study at any time and for any reason. The reasons and time for discontinuing will be recorded on CRFs, reported, and analyzed. Subjects will be terminated from the trial if the following conditions occur: (1) PD aggravates and progresses aggressively during the treatment period and investigators decide the patient needs to withdraw; (2) during the research period severe systemic disease such as an active malignant tumor, decompensated cirrhosis, or hematopoietic systems diseases are found; (3) surgery is needed due to acute abdomen, trauma, or other diseases during the treatment period; (4) voluntary withdrawal from the trial; or (5) serious complications occur, and treatment is needed.

Compliance assessment

Patients will be asked to record a diary of intervention medicine taken, and to return any remaining medicine. The compliance rate will be calculated with the following formula: Compliance rate = (actual dosage /expected dosage) × 100%. Patients with compliance rates equal to or exceeding 80% will be considered to have high compliance.

Rescue and concomitant treatment

When patients undergo unbearable pain during menstruation, painkillers (Fendid) will be given according to doctors’ orders, and the concomitant medication will be recorded. Other drugs that alleviate menstrual pain will be prohibited, such as oral contraceptives. Chinese herbal medicines that have the effect of moving Qi and activating the blood will also be prohibited.

Outcome measures

Outcome measurement time points are provided in Table 2.

Table 2 Schedule for enrollment, interventions, and assessments

Primary outcome

The primary outcome is change in the mean pain intensity as measured by the visual analog scale (VAS), from baseline to the end of treatment. The VAS rates the severity of menstrual pain from 0 to 10 cm (no pain to the most serious pain imaginable) [30]. Participants will self-rate their mean pain intensity using VAS at baseline and each visit.

Secondary outcomes

The secondary outcomes are as follows:

  • The change in menstrual pain duration

  • The change in peak pain intensity as measured by VAS

  • CM syndrome change

  • Cox Menstrual Symptom Scale (CMSS) [31]

  • Quality of life, as measured by EQ-5D-5L [32]

  • Cumulative painkiller consumption

  • Health economics

Participants will self-rate their peak pain intensity using VAS, report menstrual pain duration, and fill out CMSS at baseline and each visit. Investigators will evaluate the subjects’ CM syndrome at baseline and each visit. EQ-5D-5L will be completed by the participant at baseline, the end of treatment, and the end of the follow-up period. Health economics will be assessed at baseline and each visit of treatment duration. Investigators will look through diaries filled out by participants to confirm the painkiller consumption at every visit (see Table 2).

Safety assessment

Adverse events (AEs) experienced by the patient at any point in the trial will be reported to the investigators and recorded on the CRFs. In addition to participant self-report, physicians will inquiry the participants to seek and record any AEs that happened in the duration of the trial. Besides, abnormal laboratory findings with clinical significance will also be recorded as AEs. AE details include the time of occurrence, severity, causality to the intervention, whether the event was serious, action taken, and AE outcome. The WHO Uppsala Monitoring Centre System for Standardized Case Causality Assessment will be used to assess the causality between AEs and intervention [33]. XFZY may cause AEs such as upset stomach [34], dizziness, rash, insomnia, fever, or toothache [35]. SAEs must be reported to both the Data and Safety Monitoring Committee (DSMC) and the Ethics Committee within 24 h.

Sample size calculation

At present, no trial has compared XFZY for PD to a placebo. Therefore, we referred to Chou’s trial which studied the effect of XFZY decoction on PD and used VAS score as an outcome measure. According to Chou’s study, the mean change from baseline to the end of treatment was 4.9 ± 0.94 (mean ± SD) [34]. XFZY is a modified dosage of Xuefu Zhuyu Decoction, and the treatment in Chou’s study was added or subtracted on the basis of the pattern. Thus, we assumed that the mean change in VAS should be 3.0 ± 0.94 in the XFZY group. In a previous trial, the mean change for VAS in the placebo group was 0.88 ± 1.64 [36]. The minimal clinically important difference (MCID) for VAS was 1.6 on acute abdominal pain [37]. In this trial, the mean changes in VAS score after 12 weeks of treatment (3 menstrual cycles) for both the XFZY group and the placebo group were assumed to be 3 ± 0.94 and 0.88 ± 1.64, respectively. We set α to 0.025 and β to 0.2 and calculated as if the sample size was 105 in each group. Calculations were done with PASS (version 11.0, NCSS, LLC. Kaysville, UT, USA). Anticipating a dropout rate of 15%, we will require a sample size of 124 for each group.

Data management and quality control

Before recruitment, investigators, assessors, and research assistants will attend a training workshop to ensure they adhere to the study protocol and are familiar with the administration process. Also, standard operating procedures (SOPs) will be drafted and sent to the entire research team.

CRFs, PROs, and other resource trial data will be checked by the investigators themselves and by clinical research associates (CRA) from an independent department at Jilin Aodong Yanbian Pharmaceutical Co. Ltd. They will monitor all collected data. The GPHCM Department of Scientific Research and the Office of National Key Technology R&D Program for the Thirteen Five-year Plan of the Ministry of Science and Technology, China, will inspect the trial. The DSMC will be established before the trial in order to monitor the safety events throughout.

Data will be collected according to SOPs and entered into an electronic data capture (EDC) system developed by IBRCM. Traces of any data modification will be required to be retained. A data manager will check all the data without knowing the treatment allocation and will notify the investigator of any discrepancies. The database will be locked after all data have been checked and cleaned.

Statistical analysis

Data will be processed with PASW Statistics 18.0 (IBM SPSS Inc., Armonk, New York, USA) and SAS (SAS Institute Inc., Cary, USA). Statistical analysis will be performed by qualified statisticians who are independent from the research team and are blinded to treatment allocation. Two-tailed P values < 0.05 will be considered statistically significant. The analysis will be based on the intent-to-treat (ITT) and the per-protocol (PP) principle. The ITT population will include all participants randomized to this trial. The PP population will only include participants with neither major protocol deviations nor low compliance. Missing data will be replaced in accordance with the principle of multiple imputations. There is no plan for any interim analysis. Efficacy assessment will be analyzed by ITT and PP population, simultaneously. If these two results are inconsistent, the ITT analysis will be considered the primary result.

Demographic and other baseline data will be presented by descriptive statistics. An independent t test will compare the change in the mean pain intensity as measured by VAS from baseline to the end of the treatment, between the two groups’ primary outcomes. Superiority will be confirmed by 95% confidence intervals. For secondary outcomes, continuous and categorical data will be compared between the two groups with either a t test, chi-square test or Fisher’s exact test. Frequency, mean, standard deviation (SD), median, and range of secondary outcomes will be summarized. To analyze the factors affecting the outcome change at each time point, either a mixed-effects or a linear or logistic regression model will be performed adjusting for baseline characteristics such as age, menstrual pain severity, cumulative painkiller consumption, and other variables. The repeated measure analysis of variance will be conducted to distinguish the treatment effect and time effects. Subgroup analysis will be performed based on disease severity and age.

Safety will be assessed by AEs and ADRs and will be presented with descriptive statistics for each group. Frequency differences for AEs and ADRs will be compared with a chi-square test or Fisher’s exact test.


This protocol describes a randomized, placebo-controlled, double-blind, parallel-group multicenter trial to investigate the efficacy and safety of XFZY for primary dysmenorrhea patients with QBP according to CM. Validated evaluation tools will be used to assess dysmenorrhea severity. To our knowledge, this is the first clinical study to investigate the efficacy of XFZY for PD compared to a placebo. The use of a placebo has the advantage of preventing expectation biases resulting from inadequate blinding. Blinding of participants, personnel, and outcome assessors may reduce the risk that knowledge of which intervention was received, rather than the intervention itself, affects outcomes. When blinding is effective, a similar amount of attention and ancillary treatment between groups can be ensured. It is especially important to apply blinding to the outcome assessors to assess subjective outcomes, such as the degree of postoperative pain [38].

This study may be limited in that 3 months of treatment duration may be insufficient for complete PD pain relief. However, a systematic review of XFZY for PD [21] found that the treatment duration was 3 months (menstrual cycles) for all of the included trials, with only one exception [39]. Therefore, we believe that 3 months is a sufficient duration for observing the preliminary clinical effects of XFZY on PD and that an RCT is needed to evaluate the long-term effects.

In sum, this trial is the first study designed to demonstrate the efficacy and safety of XFZY in treating PD patients, compared with a placebo.

Trial status

The protocol version is V1.0/20190920. The trial started in January 2020 and is currently recruiting patients. It is expected to be complete in March 2021.

Availability of data and materials

Data sharing is not applicable to this article as no datasets were generated or analyzed during the current study. However, the data will be available from the corresponding authors on reasonable request after study completion.



Adverse events


Adverse drug reactions


China Food and Drug Administration


Chinese medicine


Cox Menstrual Symptom Scale


Case report form


Clinical research associates


Electronic data capture


Data and Safety Monitoring Committee


Guangdong Provincial Hospital of Chinese Medicine


Good Manufacturing Practice


China Academy of Chinese Medical Sciences


Intent-to-treat principle


Non-steroidal anti-inflammatory drug


Primary dysmenorrhea


Per-protocol principle


Qi stagnation and blood stasis pattern


Standard deviation


Serious adverse events


Serious adverse reactions


Standard operating procedures


Visual analog scale


Xuefu Zhuyu


  1. Kho KA, Shields JK. Diagnosis and management of primary dysmenorrhea. JAMA. 2019.

  2. Roger P Smith, MDAndrew M Kaunitz, MD. Dysmenorrhea in adult women: clinical features and diagnosis. Accessed 14 Jan 2020.

  3. Hu Z, Tang L, Chen L, Kaminga AC, et al. Prevalence and risk factors associated with primary dysmenorrhea among Chinese Female University students: a cross-sectional study. J Pediatr Adolesc Gynecol. 2020;331(1):15–22.

    Article  Google Scholar 

  4. Hong J, Jones M, Mishra G. The prevalence and risk factors of dysmenorrhea. Epidemiol Rev. 2014;36:104–13.

    Article  Google Scholar 

  5. The Society of Obstetricians and Gynaecologists of Canada. No.345-Primary Dysmenorrhea Consensus Guideline. J Obstet Gynaecol Can. 2017;39(7):585e595.

    Google Scholar 

  6. Marjoribanks J, Ayeleke RO, Farquhar C, et al. Nonsteroidal anti-inflammatory drugs for dysmenorrhoea. Cochrane Database Syst Rev. 2015;7:Cd001751.

    Google Scholar 

  7. Yanying W. Research progress of pathogenesis and treatment of primary dysmenorrheal. Chinese J Tradit Chinese Med. 2015;30(07):2447–9.

    Google Scholar 

  8. World Health Organization. WHO international standard terminologies on traditional medicine in the Western Pacific Region. Geneva: World Health Organization; 2007.

    Google Scholar 

  9. Xiao L, Yancang D, Yajing S, et al. Study on TCM syndromes of primary dysmenorrhea based on literature research and expert consensus. Chinese J Inform TCM. 2020;27(2):1–6.

    Google Scholar 

  10. Huiling D. The research of the distribution of TCM constitution and TCM syndrome and the correlation factors of primary dysmenorrhea patients. Chengdu: Chengdu University of Chinese medicine; 2017.

  11. Yenyu C. Distribution characteristics of traditional Chinese medicine syndromes of primary dysmenorrhea in central region of Taiwan. Jinan: Shandong University of Chinese Medicine; 2016.

  12. He H, Chen G, Gao J, et al. Xue-Fu-Zhu-Yu capsule in the treatment of qi stagnation and blood stasis syndrome: a study protocol for a randomised controlled pilot and feasibility trial. Trials. 2018;19:515.

    Article  Google Scholar 

  13. Shuagnhogn LU, Wang H. The advance in clinical application of Xuefu ZhuyTang. Hunan J Tradit Chin Med. 2020;36(10):200–2.

    Google Scholar 

  14. Park B, You S, Jung J, et al. Korean studies on blood stasis: an overview. Evid Based Complement Altern Med. 2015;2015:1–7.

    Google Scholar 

  15. Wang G. Xuefu Zhuyu Oral Liquid, a classic drug for activating blood and removing blood stasis [J]. Jilin J Tradit Chinese Med. 2004;24(08):62.

    Google Scholar 

  16. Li TF. Therapeutic effect of Xuefu Zhuyu Koufuye in the treatment of primary dysmenorrhea. Pract Clin J Integr Tradit Chin West Med. 2014;14(9):27–8.

    CAS  Google Scholar 

  17. Xu X, Wang W, Xi W, et al. An experimental study on the effect of Xuefu Zhuyu pills on activating qi and removing blood stasis. Chinese Tradit Herbal Drugs. 2006;37:74–7.

    Google Scholar 

  18. Tan Y, Zhao S, Hu Y, et al. Experimental study of Xuefu Zhuyu decoction in activating blood and removing blood stasis. Pharmacol Clini Chinese Materia Medica. 1993;05:9–10.

    Google Scholar 

  19. National Medical Products Administration. Chinese-made medicines. Accessed 14 Jan 2020.

  20. Chinese Pharmacopoeia commission. The pharmacopoeia of the People’s Republic of China 2015 edition. Beijing: China Medical Science and Technology Press; 2015. p. 849.

  21. Leem J, Jo J, Kwon CY, et al. Herbal medicine (Hyeolbuchukeo-tang or Xuefu Zhuyu decoction) for treating primary dysmenorrhea: a systematic review and meta-analysis of randomized controlled trials. Medicine (Baltimore). 2019;98(5):e14170.

    Article  Google Scholar 

  22. Li TF. Therapeutic effect of Xuefu Zhuyu liquid in the treatment of primary dysmenorrhea. Pract Clin J Integr Tradit Chin West Med. 2014;14(9):27–8.

    CAS  Google Scholar 

  23. Huang Y. Xuefu Zhuyu decoction in the treatment of primary dysmenorrhea. Inf Tradit Chin Med. 2014;31(2):95–6.

    Google Scholar 

  24. Wang YX. Therapeutic effect of modified Xuefu Zhuyu decoction in the treatment of primary dysmenorrhea with qi stagnation and blood stasis. Chin J Clin Ration Drug Use. 2015;8(6c):135–6.

    Google Scholar 

  25. Zhao DK. Therapeutic effect of modified Xuefu Zhuyu decoction in the treatment of dysmenorrhea. Nei Mong J Tradit Chin Med. 2016;6:13–4.

    Google Scholar 

  26. Wang HY. 120 cases of primary dysmenorrhea treated with combination of traditional Chinese medicine and Western medicine. China Health Care Nutr. 2013;23(6):3424.

    Google Scholar 

  27. Wu JP, Kang ZY. Clinical study on primary dysmenorrhea treated with combination of traditional Chinese medicine and Western medicine. China J Chin Med. 2014;29(6):896–7.

    Google Scholar 

  28. Chou YF. Therapeutic effect of modified Xuefu Zhuyu decoction in the treatment of dysmenorrhea with qi stagnation and blood stasis. J Sichuan Tradit Chin Med. 2015;33(5):117–8.

    Google Scholar 

  29. Wang J, An Y, Li ZL, et al. Development of PRO scale for qi stagnation and blood stasis syndrome. Chinese J Exp Tradit Med Formulae. 2018;24(15):16–20.

    Google Scholar 

  30. Maria CA. Assessment of chronic pain. I. Aspects of the reliability and validity of the visual analogue scale. Pain. 1983;16:87–101.

    Article  Google Scholar 

  31. Cox DJ, Meyer RG. Behavioral treatment parameters with primary dysmenorrhea. Behav Med. 1978;1(3):297–310.

    Article  CAS  Google Scholar 

  32. Janssen MF, Pickard AS, Golicki D, et al. Measurement properties of the EQ-5D-5L compared to the EQ-5D-3L across eight patient groups: a multi-country study [J]. Qual Life Res. 2013;22(7):1717–27.

    Article  CAS  Google Scholar 

  33. WHO. The use of the WHO-UMC system for standardised case causality assessment. Accessed 14 Jan 2020.

  34. Yanfei Q. Clinical observation on the effect of Xuefu Zhuyu decoction in treating dysmenorrhea with qi stagnation and blood stasis. Sichuan Tradit Chinese Med. 2015;33(05):117–9.

    Google Scholar 

  35. Guang C. Efficacy and full transcriptome mechanism of medicine for qi stagnation and blood stasis syndromes. Beijing: Beijing University of Traditional Chinese Medicine; 2019.

  36. Park JS, Park S, Cheon CH, et al. Effects and safety of gyejibongnyeong-hwan on dysmenorrhea caused by blood stagnation: a randomized controlled trial. Evid Based Complement Alternat Med. 2013;2013:424730.

    PubMed  PubMed Central  Google Scholar 

  37. Gao W, Wang X. Research progress of visual analog pain score [J]. J Med Res. 2013;42(12):144–6.

    Google Scholar 

  38. JPT H, Altman DG, Sterne JAC. Chapter 8: Assessing risk of bias in included studies. In: Higgins JPT, Churchill R, Chandler J, Cumpston MS, editors. Cochrane handbook for systematic reviews of interventions version 5.2.0 (updated June 2017), Cochrane, 2017. Available from Accessed 14 Jan 2020.

  39. Xu W. Progress in clinical and experimental research of Xuefu Zhuyu decoction. Guangming J Tradit Chinese Med. 2013;28(03):635–7.

    Google Scholar 

Download references


The authors thank Professor Hongyan Yang from the Department of Gynecology at GPHCM for her professional advice on our protocol.


This trial is supported by a grant from the National Key Research and Development Program of China (No. 2018YFC1707407). The funder had no role in the design of the study; in the collection, analyses, or interpretation of the data; in the writing of the article; or in the decision to publish the results.

Author information

Authors and Affiliations



GL and ZZ: drafting of the manuscript. GL, XW, and ZW: conception, design, and final approval of the manuscript. LZ, SL, JS, and YL: design and critical revision. ZW: securing funding and supervising the work. All authors read and approved the final version of the manuscript prior to submission.

Authors’ information

Not applicable.

Corresponding authors

Correspondence to Xin Wang or Zehuai Wen.

Ethics declarations

Ethics approval and consent to participate

The Ethics Committee at Guangdong Provincial Hospital of Chinese Medicine approved this trial. The permission number is BF2019-175-01. Informed consent will be obtained from all participants. All personal information about potential and enrolled participants will be confidential.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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 The Creative Commons Public Domain Dedication waiver ( 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

Li, G., Zhang, Z., Zhou, L. et al. Chinese herbal formula Xuefu Zhuyu for primary dysmenorrhea patients (CheruPDYS): a study protocol for a randomized placebo-controlled trial. Trials 22, 95 (2021).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: