drugset / Trial / NCT00490308

The Influence of Estradiol Supplementation During the Luteal in Patients Undergoing IVF Treatment

NCT00490308

Phase 1 Unknown 120 enrolled Assaf-Harofeh Medical Center
RandomizedCrossoverOpen-labelTreatment

Summary

To evaluate whether treatment with Estradiol supplementation during the luteal phase improves IVF outcomes Patients undergoing IVF treatment with controlled ovarian hyperstimulation using a GnRH analog will receive 4 mg estradiol valerate in the luteal phase.Patient's followup will include E2 progesterone and BHCG 14 days after embryo transfer and vaginal ultrasound on day 21 and 28 after embryo transfer

Timeline

Start
2007-08
Primary completion
Completion
2008-08

Drugs

EvaluationDrugModalityDoseRoute
Subject estradiol valerate Unknown 4 mg Oral

Indications