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Clinical Trial Summary

The study aims to evaluate the effect of an increased dose of vaginal progesterone supplementation on the incidence of ongoing pregnancy for patients with a suboptimal serum progesterone level (defined as < 10 mcg/l) on the day of blastocyst transfer.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04806919
Study type Interventional
Source University Hospital, Ghent
Contact
Status Recruiting
Phase Phase 3
Start date April 2, 2021
Completion date January 1, 2025

See also
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