Investigation of the effect of chamomile on ovulation induction in patients with polycystic ovary syndrome
Phase 2
Recruiting
- Conditions
- Polycystic ovarian syndrome.Polycystic ovarian syndrome
- Registration Number
- IRCT20170315033085N3
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 70
Inclusion Criteria
Normal maturation
Thyroid test is within normal range
Having Rotterdam criteria for polycystic ovary syndrome
Patient's age is between 18 and 35
Not having a recent history of surgical treatment and other treatment for polycystic ovary syndrome
Exclusion Criteria
Use of sex steroids (such as birth control pills, hormone therapy, androgenic drugs)
Use of chemical or herbal medicine
Use of cigarettes or hookahs
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Rate of ovulation induction in patients with polycystic ovary syndrome. Timepoint: Investigate of the ovarian follicles is done on 12th day of the first cycle and also on the 3rd and 12th days of the third cycle and in case of not having menstruation, at the end of 90th for all patinets. Method of measurement: Transvaginal ultrasound.;Total testostrone rate. Timepoint: measuring testostrone rate at the beginning of the study (before intervention) and at the end of the study. Method of measurement: ELISA method.
- Secondary Outcome Measures
Name Time Method