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
| Type | Name | Description |
|---|---|---|
| DRUG | Ganirelix | sc 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.