Trials / Completed
CompletedNCT00780858
Premature Luteinization Prevention by GnRH Antagonist in Patients Undergoing IUI
GnRH Antagonist Prevention of Premature Luteinization in Patients Undergoing IUI
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 662 (actual)
- Sponsor
- IVI Madrid · Academic / Other
- Sex
- Female
- Age
- 18 Years – 40 Years
- Healthy volunteers
- Not accepted
Summary
Premature luteinization in patients undergoing IUI can occur in up to 24% of cycles. These patients, according to recent data, have a lower pregnancy rate than controls. The possibility to avoid premature luteinization with GnRH antagonist may restore the chances of achieving a pregnancy in these women.
Detailed description
The purpose of this study was to investigate whether a subset of patients benefits from GnRHa administration during IUI. PL was tested for in patients who were undergoing artificial insemination procedures, and the effect of GnRHa on PR in patients who
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ganirelix | Ganirelix 0.25mg s.c every 24 h starting stimulation day 6 |
Timeline
- Start date
- 2008-10-01
- Primary completion
- 2010-12-01
- Completion
- 2011-03-01
- First posted
- 2008-10-28
- Last updated
- 2015-05-06
Locations
1 site across 1 country: Spain
Source: ClinicalTrials.gov record NCT00780858. Inclusion in this directory is not an endorsement.