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Clinical Trial Summary

The current study, aims through a robust design to provide a simple answer on whether progesterone levels of the same individual may significantly vary depending on the time of blood retrieval before the ovulation triggering, by evaluating the daily variability of serum progesterone on the day of triggering in healthy women who perform a COS for oocyte donation, through multiple blood samplings.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03366025
Study type Observational [Patient Registry]
Source Institut Universitari Dexeus
Contact
Status Completed
Phase
Start date November 1, 2017
Completion date January 25, 2018

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