Clinical Trials Directory

Trials / Completed

CompletedNCT04722471

Progesterone Levels and Clinical Outcomes Using a Single Pessary of 400 mg of Vaginal Progesterone in Substitutive Cycles for Embryo Transfer.

Status
Completed
Phase
Study type
Observational
Enrollment
347 (actual)
Sponsor
Instituto Bernabeu · Academic / Other
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

This study aims to compare the efficacy, in terms of progesterone levels and clinical outcomes, of two different presentations of micronized vaginal progesterone (400 mg vs. 200 mg) used in endometrial preparation in artificial cycle (AC) for embryo transfer. This is a non-inferiority, retrospective case-control study, with at least 200 cycles analyzed (at least 100 per arm) and the primary outcome is the serum progesterone level on the day of the embryo transfer.

Conditions

Interventions

TypeNameDescription
DRUGVaginally administered progesteroneThe artificial endometrial preparation for an embryo transfer with the use of 400 mg vaginal tablet (one tablet twice a day) or 200 mg (two tablets twice a day)

Timeline

Start date
2021-03-03
Primary completion
2021-03-03
Completion
2021-03-17
First posted
2021-01-25
Last updated
2021-03-19

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT04722471. Inclusion in this directory is not an endorsement.