Clinical Trials Directory

Trials / Completed

CompletedNCT00750100

Low Dose hCG in the Late Follicular Phase

Among ICSI Patients Undergoing Antagonist Protocols With Recombinant FSH, Does Replacement of Recombinant FSH by 200 IU of hCG in the Late Follicular Phase Compared With Continuing Recombinant FSH, Result in a Similar Number of Oocytes?

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
70 (actual)
Sponsor
Universitair Ziekenhuis Brussel · Academic / Other
Sex
Female
Age
18 Years – 36 Years
Healthy volunteers
Not accepted

Summary

In this study,the investigators compared two protocols for controlled ovarian hyperstimulation in infertility patients requiring IVF. In the control group, the patient undergoes a standard antagonist protocol. In the study group, the administration of gonadotropins is stopped in the late follicular phase and replaced by low dose human chorionic gonadotropins. The primary endpoint of the study is the number of oocytes retrieved in both groups.

Conditions

Interventions

TypeNameDescription
DRUGhuman chorionic gonadotropinhCG 200IU in the late follicular phase
DRUGrecombinant gonadotropins200 IU per day during controlled ovarian stimulation

Timeline

Start date
2007-09-01
Primary completion
2008-01-01
Completion
2008-11-01
First posted
2008-09-10
Last updated
2010-10-11

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT00750100. Inclusion in this directory is not an endorsement.

Low Dose hCG in the Late Follicular Phase (NCT00750100) · Clinical Trials Directory