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
| Type | Name | Description |
|---|---|---|
| DRUG | human chorionic gonadotropin | hCG 200IU in the late follicular phase |
| DRUG | recombinant gonadotropins | 200 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.