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The clinical study of Jiawei Mojie Tablet in the treatment of endometriosis-related dysmenorrhea with qi stagnation and blood stasis.

The clinical study of Jiawei Mojie Tablet in the treatment of endometriosis-related dysmenorrhea with qi stagnation and blood stasis.

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078100
Enrollment
Unknown
Registered
2023-11-28
Start date
2023-07-27
Completion date
Unknown
Last updated
2023-12-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometriosis

Interventions

Test Group:Jiawei Mojie Tablet
Placebo Group:placebo

Sponsors

Yueyang integrated traditional Chinese and Western Medicine Hospital Affiliated to Shanghai University of traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1.Meet the diagnostic criteria of endometriosis-related dysmenorrhea. 2.Meet the syndrome differentiation requirements of qi stagnation and blood stasis syndrome. 3.The maximum VAS score for dysmenorrhea within the last 3 menstrual cycles =4. 4.Patients who have regular menstrual cycles (21-35 days) with periods for 3-7 days. 5.Age =20 years and =40 years. 6.Understand, agree to participate in this study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients who suffer from primary dysmenorrhea, ovarian malignant carcinoma, adenomyosis and chronic pelvic inflammatory disease and so on. 2.Patients who have used medicine or other therapies (including laparoscopy) for endometriosis or traditional Chinese medicine and Chinese patent medicine with the efficacy of regulating qi and removing blood stasis within the last 3 months. 3.The diameter of ovarian endometrioma = 5cm. 4.SCr > the upper limit of normal, ALT or AST = 1.5 times the upper limit of normal, or hemoglobin = 90g/L. 5.Patients who have used long-acting contraceptive injections or implants within the last 6 months. Patients who have used contraceptives or medicated intrauterine devices within the last 8 weeks. And patients who are going to prepare for pregnancy within half a year as well as patients who are in pregnancy or in lactation. 6.Patients who complicate with heart, liver, kidney or other serious primary diseases, and patients who are psychopaths. 7.Patients who are suspected or confirmed to have the history of alcoholic abuse or drug abuse. 8.Patients who are suspected or confirmed to be allergic to ingredients or auxiliary materials of experimental drugs and emergency drugs. 9.Patients who have participated in or are currently participating in other clinical trials within the last 3 months.

Design outcomes

Primary

MeasureTime frame
The mean VAS score for dysmenorrhea after 3 treatments;

Secondary

MeasureTime frame
The maximum VAS score for dysmenorrhea;The hours of VAS score=4 during a menstrual cycle;The CMSS score of dysmenorrhea syndromes severity;The CMSS score of dysmenorrhea syndromes duration;TCM syndrome score;Menstruation characteristics score;Tumor markers (CA125 and CA199);Uterine and adnexal ultrasound;The Endometriosis Health Profile-5;

Countries

China

Contacts

Public ContactDong Li

Yueyang integrated traditional Chinese and Western Medicine Hospital Affiliated to Shanghai University of traditional Chinese Medicine

yyyydongli@163.com+86 189 3056 5213

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026