Clinical Trials Directory

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

TypeNameDescription
DRUGGanirelixGanirelix 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.

Premature Luteinization Prevention by GnRH Antagonist in Patients Undergoing IUI (NCT00780858) · Clinical Trials Directory