Infertility Clinical Trial
Official title:
Administration of a GnRH Antagonist During 3 Days at Initiation of the Cycle: Impact on the Stimulation in IVF/ICSI
Verified date | November 2009 |
Source | Universitair Ziekenhuis Brussel |
Contact | n/a |
Is FDA regulated | No |
Health authority | Belgium: Institutional Review Board |
Study type | Interventional |
In this prospective study, the investigators would like to show whether ovarian stimulation with pretreatment of a GnRH antagonist during 3 consecutive days at initiation of the cycle, is possible.
Status | Completed |
Enrollment | 70 |
Est. completion date | May 2010 |
Est. primary completion date | May 2010 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 39 Years |
Eligibility |
Inclusion Criteria: - < 39 years old on day of randomisation - FSH < 12 (in the early follicular phase) - Normal ultrasound scan, i.e. presence of both ovaries, without evidence of abnormality within 6 months prior to randomisation. - Regular menstrual cycles of 21-35 days, presumed to be ovulatory. - BMI between 18 and 29 (both inclusive) - 1st or 2nd trial - IVF or ICSI - Randomisation at out-patient clinic Exclusion Criteria: - = 39 years old on day of randomisation - Endometriosis = grade 3 - PCOS |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Belgium | UZ Brussel | Jette | Brussels |
Lead Sponsor | Collaborator |
---|---|
Universitair Ziekenhuis Brussel |
Belgium,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Endocrine profile | The purpose is to assess the endocrine profile in each treatment group | up to 9 months | No |
Secondary | Pregnancy rate | The purpose is to study the pregnancy rate in each treatment group | up to 9 months | No |
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