Polycystic ovarian syndrome. Polycystic ovarian syndrome
Conditions
Interventions
Intervention 1: Intervention group: Patients daily receive two 500-mg chamomile capsules for 3 months. Intervention 2: Control group: Patients daily receive two placebo capsules (which are similar to
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAzam Akbari Lor
Mashhad University of Medical Sciences
Outcome results
None listed