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Clinical Study on the Treatment of Ovarian Endometriosis Using a Method Based on the "Blood-Water Theory" to Promote Blood Circulation, Remove Blood Stasis, Enhance Water Metabolism, and Dissolve Masses

Clinical Study on the Treatment of Ovarian Endometriosis Using a Method Based on the "Blood-Water Theory" to Promote Blood Circulation, Remove Blood Stasis, Enhance Water Metabolism, and Dissolve Masses

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000252
Enrollment
Unknown
Registered
2026-02-03
Start date
2024-01-01
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Endometriosis

Interventions

Control group:Dydrogesterone (China Resources, National Drug Approval Number H20213831, 2mg/day, oral).
Study group:Guizhi Fuling Pill with modifications, taken orally, one dose daily, to be taken warm in the morning and evening.

Sponsors

The First Affiliated Hospital of Hunan University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: According to Chinese and Western medical diagnostic criteria, the inclusion standards for OEM phlegm-stasis mutual entanglement syndrome are established as follows: (1) Meets Western medical diagnostic criteria for OEM; (2) Meets Chinese medical diagnostic and pattern differentiation criteria for phlegm-stasis mutual entanglement syndrome; (3) Concurrent ovarian endometriotic cysts with diameter <4cm; (4) Malignant transformation of endometriosis excluded; (5) Reproductive-age women with no desire for pregnancy within the next year or who have completed their family planning; (6) Patients requesting Chinese herbal medicine management and signing an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Concurrent malignant tumours, immune system disorders, cardiovascular or cerebrovascular diseases, chronic pulmonary conditions, abnormal liver or renal function, psychiatric disorders, gastrointestinal dysfunction, or hysterectomy, pregnancy, and lactation; (2) Patients with prior ineffective drug therapy; (3) Use of hormonal medications within three months prior to consultation (e.g., contraceptives, progestogens, GnRH-a agonists, etc.). (4) Other circumstances rendering the patient unsuitable for inclusion.

Design outcomes

Primary

MeasureTime frame
Peak pain intensity VAS score;Traditional Chinese Medicine Syndrome Scoring;The maximum diameter of the ovarian cyst;

Secondary

MeasureTime frame
Total Duration Score for Dysmenorrhea;Overall Symptom Relief Rating;Levels of angiogenesis and tumor markers;Serum Immunological Markers and Inflammatory Cytokine Testing;Serum Hormone Level Testing;Ovarian Reserve Function Assessment;

Countries

China

Contacts

Public ContactLuo xi

The First Affiliated Hospital of Hunan University of Traditional Chinese Medicine

278765670@qq.com18408284178

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Mar 14, 2026