Clinical Trials Directory

Trials / Completed

CompletedNCT00461422

Early Follicular Supplementation of Ganirelix in IVF 2004

Early Follicular GnRH Antagonist Supplementation Improves Fertilization and Embryo Cleavage Rates in IVF-ET GnRH Antagonist Cycles

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
50 (actual)
Sponsor
The Baruch Padeh Medical Center, Poriya · Other Government
Sex
Female
Age
Healthy volunteers
Not accepted

Summary

Our goal was to investigate whether early follicular supplementation of the GnRH antagonist to the flexible GnRH antagonist protocol, has a potential to improve IVF-ET clinical results

Detailed description

GnRH antagonist offers many advantages when used in IVF-ET treatment, however, it is suspected to yield lower pregnancy rate when compared with the long GnRH agonist protocol. Our goal was to investigate whether early follicular supplementation of the GnRH antagonist to the flexible GnRH antagonist protocol, has a potential to improve IVF-ET clinical results. Consecutive patients are prospectively enrolled and randomly assigned to the study and control groups. Patients with low ovarian reserve or with uterine distortion are excluded from the study. Both groups are treated with recombinant FSH and the flexible GnRH antagonist protocol. Women in the study group are also treated with additional GnRH antagonist 0.25 mg/day on day 1, 2 and 3 of the menstrual cycle.

Conditions

Interventions

TypeNameDescription
DRUGGanirelixsc injection of Ganirelix 0.25 mg per day

Timeline

Start date
2004-01-01
Primary completion
2007-06-01
Completion
2007-06-01
First posted
2007-04-18
Last updated
2008-06-27

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT00461422. Inclusion in this directory is not an endorsement.