polycystic ovarian syndrome. Polycystic ovarian syndrome
Conditions
Interventions
Intervention 1: Control group: group A received letrozole tablet ( abouraihan , Iran ) 5 mg from day 3 of menstrual cycle for 5 days .They were monitored hormonal and Sonographical on day 3 and day 1
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
20 Years to 35 Years
Inclusion criteria
Inclusion criteria: AGE: 25-35 years at least one patent Fallopian tube normal sperm analysis of spouse presence of poly-cystic ovarian syndrome
Exclusion criteria
Exclusion criteria: Smoking underlying disease ( heart, kidney, liver or Endocrine)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Luteinizing hormone. Timepoint: Third and 12th day of menstrual cycle. Method of measurement: laboratory Test.;Testestron. Timepoint: Third and 12th day of menstrual cycle. Method of measurement: laboratory Test.;Anderestandion. Timepoint: Third and 12th day of menstrual cycle. Method of measurement: laboratory Test.;Esteradiol. Timepoint: Third and 12th day of menstrual cycle. Method of measurement: laboratory Test.;Pregnancy. Timepoint: 14 days after Intrauterine insemination. Method of measurement: laboratory Test, pregnancy test. | — |
Secondary
| Measure | Time frame |
|---|---|
| Dominant follicles. Timepoint: 12th day of Menestural cycle. Method of measurement: vaginal Sonography.;Endometrium thickness. Timepoint: 12th day of Menestural cycle. Method of measurement: vaginal Sonography. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMalihe Afiat
Mashhad University of Medical Sciences
Outcome results
None listed