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Clinical Trial Summary

Our aim is to access whether we can achieve equivalent pregnancy rates by the addition of six doses of luteal support with recLH after agonist triggering for IVF cycles in the absence of OHSS.


Clinical Trial Description

Whether pregnancy outcome after GnRH-agonist triggering could be improved by adding luteal recLH support plus progesterone, compared to that observed after ovulation triggering with HCG in GnRH antagonist stimulated cycles. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00954811
Study type Interventional
Source Universitair Ziekenhuis Brussel
Contact Evangelos Papanikolaou, PhD
Email drvagpapanikolaou@yahoo.gr
Status Recruiting
Phase Phase 4
Start date September 2005
Completion date December 2010

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