Bariatric Subfertility Trial
- Conditions
- SubfertilityPCOSMorbid obesityBariatric surgeryLife style modification
- Registration Number
- NL-OMON29279
- Lead Sponsor
- J.S.E. Laven, MD, PhDErasmus Medical CenterDepartment of Department of Reproductive Endocrinology3000 CA Rotterdam, The Netherlands
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 240
Inclusion Criteria
•Age 18-40 years
•BMI > 35 kg/m2.
Exclusion Criteria
•Azoospermia, endometriosis AFS class > III, WHO class III anovulation (premature ovarian failure) or endocrinopathies (such as Cushing syndrome, adrenal hyperplasia and diabetes type I).
•Pregnancy induced hypertension, preeclampsia, eclampsia or HELPP syndrome in a previous pregnancy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary endpoint is the rate of healthy born baby rate after at least 37 weeks of gestation (primary end point) within three years after therapy.
- Secondary Outcome Measures
Name Time Method