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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04722471
Study type Observational
Source Instituto Bernabeu
Contact
Status Completed
Phase
Start date March 3, 2021
Completion date March 17, 2021

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