At High-risk for Pre-eclampsia After Assisted Reproductive Technology

Recruiting Observational Study
Pre-Eclampsia
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 – 48
Sex
Female
Study type
Observational
Participants needed
1,050 (estimated)
Sponsor
CRG UZ Brussel · Other
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About This Trial
The overarching goal of the project is to unravel PE etiopathogenesis in high-risk patients (PCOS patients and oocyte acceptors) after assisted reproductive technology (ART) to individualize prenatal care following ART and to determine potential targets for new PE prevention options decreasing the morbidity/mortality caused by this pathology. More specifically, the following objectives/work packag…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * First time oocyte acceptors Or Nulliparous PCOS patients undergoing ART (IVF/ICSI) * Criteria for PCOS: two out of the three following criteria must be present: 1. Oligo-or anovulation: a menstrual cycle \>35 days 2. Hyperandrogenism: * Clinically: the presence of h…
Contacts

Study nurses Brussels IVF

+32 2 477 66 99

studieverpleegkundigen_crg@uzbrussel.be

CONTACT