Clinical Trials Directory

Trials / Completed

CompletedNCT05954962

Efficacy of Micronized Natural Progesterone vs GnRH Antagonist in the Prevention of LH Peak During Ovarian Stimulation.

Evaluation of the Efficacy of Micronized Natural Progesterone (Seidigestan®) vs GnRH Antagonist (Astarté®) in the Prevention of LH Peak During Controlled Ovarian Stimulation: a Randomized Clinical Trial.

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
150 (actual)
Sponsor
Instituto Bernabeu · Academic / Other
Sex
Female
Age
18 Years – 33 Years
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGProgesterone 200 MGThe patients in the study group will administer oral natural micronized progesterone capsules from day 1 of ovarian stimulation instead of "antagonist" (ganirelix) subcutaneaous injections from day 5-6 of stimulation.
DRUGGanirelix AcetateThe patients in the control group will administer subcutaneaous injections of ganirelix from day 5-6 of stimulation as per currently used protocol.

Timeline

Start date
2023-12-23
Primary completion
2025-04-03
Completion
2025-08-30
First posted
2023-07-20
Last updated
2026-03-27

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT05954962. Inclusion in this directory is not an endorsement.