A single-center non-blinded randomized controlled trial on the effect of ovarian hyperstimulation on endometrial receptivity.
Completed
- Conditions
- Subfertility or infertility
- Registration Number
- NL-OMON24197
- Lead Sponsor
- Zorgonderzoek Nederland (ZonMw)
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 193
Inclusion Criteria
Subfertile couples with female age <43 undergoing IVF (in vitro fertilization) or ICSI (intracytoplasmatic sperm injection).
Exclusion Criteria
1. Couples undergoing a PGD cycle;
2. Couples for which IVF/ICSI is used to prevent the transmission of HIV;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome measure will be cumulative ongoing pregnancy rate per cycle after twelve months of treatment.
- Secondary Outcome Measures
Name Time Method Secondary outcome measures will be embryo quality, clinical pregnancy rate, miscarriage rate, live birth rate, time to pregnancy, birth weight and percentage of children with congenital abnormalities.