MedPath

Comparison of oral dydrogestrone with vaginal progesterone

Not Applicable
Conditions
luteal-phase support in IVF cycles.
Complication associated with artificial fertilization, unspecified
Registration Number
IRCT2013050713265N1
Lead Sponsor
Infertility and Reproductive Health Research Center (IRHRC), IVF center,Shahid Beheshti University o
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
80
Inclusion Criteria

inclusion criteria: male factor infertility; euthyroid; normoprolactinemic. .
exclusion criteria: tubal factor infertility; idiopathic infertility; endometriosis-related infertility and ovulatory disturbances; baseline FSH >12 IU; adenomyosis; uterine myoma; chronic hepatorenal disease.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Clinical pregnancy. Timepoint: six weeks following intervention. Method of measurement: sonography and pregnancy test.;Abortion. Timepoint: six weeks following intervention. Method of measurement: sonography and pregnancy test.
Secondary Outcome Measures
NameTimeMethod
uteal-phase duration. Timepoint: 2 weeks following intervention. Method of measurement: patient history.
© Copyright 2025. All Rights Reserved by MedPath