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Comparison of Clomiphene and Letrozole in association with Metfomin in patients with anovulatio

Phase 3
Conditions
Infertility.
Polycystic ovarian syndrome
Registration Number
IRCT138807262604N1
Lead Sponsor
Research and clinical center for infertility, Shahid Sadoughi university of medical sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
100
Inclusion Criteria

polycystic ovary syndrome, Clomiphene resistant, normal liver function, normal kidney function, normal thyroid function. Exclusion criteria: use of Clomiphene in previous 2 months, use of metformin in previous 2 months.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Endometrial thickness on day of HCG administration. Timepoint: one time in each cycle. Method of measurement: distance between two layer endometrium measured by sonography.;Estrogen level on day of HCG administration. Timepoint: one time in each cycle. Method of measurement: measurement of estrogen in serum.;Number of follicles>18mm. Timepoint: every other day from cycle day 12. Method of measurement: by counting of follicles more than18 millimeter in sonography.;Chemical pregnancy. Timepoint: 2 weeks after IUI. Method of measurement: by measurement of HCG level in serum.;Clinical prgnancy. Timepoint: one time in each cycle. Method of measurement: observation of gestational sac in sonography.
Secondary Outcome Measures
NameTimeMethod
Abortion rate. Timepoint: one time in each treatment cycle. Method of measurement: observation of expulsion of product of conception from uterous, disappearance of gestational sac in sonography, HCG level in serum dropped or become negative.
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