drugset / Trial / NCT01218386

Pretreatment With Estradiol Valerate

NCT01218386

Phase 4 Completed 80 enrolled University Hospital Brussels
RandomizedParallel-groupSingle-blindTreatment

Summary

The present study is set up to evaluate the efficacy of a programmation by administration of estrogen valerate during 6 or more consecutive days. In this prospective randomised trial, we study the impact of administration of Progynova® during 6, 7,8 9 or 10 consecutive days during the luteo-follicular transition period of the menstrual cycle.

Timeline

Start
2010-05
Primary completion
2012-01
Completion
2012-01

Drugs

EvaluationDrugModalityDoseRoute
Subject estradiol valerate Unknown 2 mg Oral

Indications