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Clinical Trials/IRCT201206072967N4
IRCT201206072967N4
Completed
Phase 2

Evaluation of efficacy of vaginal progesterone on pregnancy rate in women with polycystic ovarian syndrome using combination therapies for ovulation induction

Vice chancellor of research, Kashan University of Medical Sciences0 sites200 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Infertility and Polycystic Ovarian Syndrome.
Sponsor
Vice chancellor of research, Kashan University of Medical Sciences
Enrollment
200
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Vice chancellor of research, Kashan University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • Inclusion criteria consist 20 \-35 years, having Rotterdam criteria (having 2 from 3 following criteria: Oligomenorrehea or amenorrhea, polycystic ovaries in sonography, clinical or biochemical evidences of hyperandrogenism). The patient with abnormal hormonal assay in the third day of menstruation (including FSH, TSH, prolactin, 17 Hydroxy progesterone and testosterone), tubal obstruction in HSG or laparoscopy and infertility due to male factor will be excluded.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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