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Trials / Completed

CompletedNCT00478504

Letrozole Versus Clomifene Citrate for Ovulation Induction

Double Blind Cross-over Randomized Controlled Trial Comparing Letrozole Versus Clomifene Citrate for Ovulation Induction in Women With Polycystic Ovarian Syndrome

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
159 (actual)
Sponsor
University of Nottingham · Academic / Other
Sex
Female
Age
18 Years – 39 Years
Healthy volunteers
Not accepted

Summary

The primary aim of the study is to assess the efficacy of letrozole as an ovulation induction agent and to test the hypothesis that letrozole will generate better pregnancy rates with fewer multiple pregnancies and higher live birth rate than the current standard agent, clomifene citrate in anovular infertile women with polycystic ovarian syndrome.

Conditions

Interventions

TypeNameDescription
DRUGLetrozoleStarting daily dose 2.5 mg on menstrual cycles days 2 to 6, to be increased to 5 mg daily if there is no response to 2.5 mg
DRUGClomifene citrateStarting daily dose 50 mg on menstrual cycles days 2 to 6, to be increased to 100 mg daily if there is no response to 50 mg

Timeline

Start date
2007-05-01
Primary completion
2014-06-01
Completion
2014-09-01
First posted
2007-05-24
Last updated
2016-10-28

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT00478504. Inclusion in this directory is not an endorsement.

Letrozole Versus Clomifene Citrate for Ovulation Induction (NCT00478504) · Clinical Trials Directory