drugset / Trial / NCT01200537

Optimizing Ovulation Induction in the Poor Responder

NCT01200537

RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this randomized controlled trial is to compare the efficacy and effect of luteal estradiol and combined oral contraceptive pills (COPC) on follicle recruitment and synchrony in a poor responder population. The randomized groups consist of: 1. patients receiving luteal estradiol prior to ovulation induction; and 2. patients receiving COCPs for 1 month prior to ovulation induction. Follicle characteristics and serum biomarkers will be followed and compared in each group. Coefficient of variation will be used to evaluate follicle size discrepancy. Chi square analysis will be used to compare categorical variables between treatment groups. Both estradiol and COPCs are used clinically in assisted reproduction, so this study affords no additional risks to the participants.

Timeline

Start
2010-10
Primary completion
2011-10
Completion
2012-10

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Estradiol Other / unclassified 0.1 mg Other
Comparator Loestrin Unknown Oral