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The study of the intervention and effectiveness evaluation of traditional Chinese medicine for difficult and complicated diseases

Clinical study and effectiveness evaluation of Chinese herbal medicine for pelvic endometriosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-10000808
Enrollment
Unknown
Registered
2010-03-10
Start date
2006-10-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

pelvic endmetriosis

Interventions

Group A:GnRH-a, 3.75mg, hypodermic injection or intramuscular injection, once a month. Or gestrinone 2.5 mg, twice a week
Group B:oral medication of Chinese herbal medicine, qd

Sponsors

Department of Science and Technology, State Administration of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: (1) meet the diagnose standards and TCM standars of pelvic endometriosis; (2) no history of serious drug allergy; (3) no history of surgery or laparoscopic operation due to pelvic endometriosis; (4) no medication for this desease in the previous 6 months before the operation; (5) no history of serious primary diseases such as cardiovascular and cerebrovascular diseases, liver diseases, kidney diseases or hematopoietic system diseases, no history of mental diseases; (6) women without lactation; (7) aged from 18 to 45; (8) the clinical classification belongs to ovarian endometriosis (endometrial cyst) and/or deep infiltrating endometriosis (the depth of lesions infiltration >=5mm, usually seen in the areas of utero-sacral ligament, douglas pouch, vaginal fornix and vagina-rectum); (9) patients recieved the first conservative surgery for pelvic endometriosis would be grouped during the 1-5th day of first menstruation; (10) patients sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) complicated with adenomyosis; (2) medication due to this disease after the operation or before the group allocation.

Design outcomes

Primary

MeasureTime frame
CA125;B-ultrasonic scan;Chronic Pelvic Pain Scor;

Secondary

MeasureTime frame
Menstruation Score;Gestational conditions;Whole Body Symptoms Score;Dysmenorrhea Score;

Contacts

Public ContactRuihua Zhao
rhzh801@sohu.com+86 13621021092

Outcome results

None listed

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