IRCT2016052528080N1
Completed
Phase 3
Comparing the efficacy of cupping method and medroxyprogesterone acetate in reducing menstrual bleeding in women with heavy menstrual bleeding
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- DUB.
- Sponsor
- Tehran university of Medical Sciences
- Enrollment
- 162
- Status
- Completed
- Last Updated
- 8 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •women with uterine bleeding disorders; Patients referred by a gynecologist with disorders of uterine bleeding; patient with completed informed consent form
- •Exclusion criteria: women younger than 20 or older than 50 years; history of chest surgery in the last three months; active systemic infection disease; active infected edema on Skin or injury on cupping site; coagulation disorders; use of bleeding\-lowering drugs such as Mefenamic acid, etc. during the study period; uterine fibrosis with endometrial thickness; fraction in the chest area ,especially in the ribs 7\-12 on cupping site; chemical medicines or herbal and other alternative medicine methods used during the study; pregnant or plan to become pregnant during the study; dependence on drugs in the past 6 months
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Not specified
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