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Clinical Trial Summary

This study aims to investigate if the use of oral micronized natural progesterone is not inferior to the use of subcutaneous antagonist in preventing LH peak in controlled ovarian stimulation.


Clinical Trial Description

The study will aim to include 150 women (egg donors): 75 per group and the principal variable will be the number of retrieved mature (MII) oocytes. Randomized, prospective, controlled, single center, phase IV study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05954962
Study type Interventional
Source Instituto Bernabeu
Contact Anna Pitas, PhD
Phone +34663926079
Email apitas@institutobernabeu.com
Status Not yet recruiting
Phase Phase 4
Start date October 23, 2023
Completion date September 30, 2024

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