What Are the Predictive Factors for Preeclampsia in Oocyte Recipients? - PREROVE
Completed
- Conditions
- Oocyte DonationPregnancy
- Registration Number
- NCT03668184
- Lead Sponsor
- Rennes University Hospital
- Brief Summary
The main goal is to determine which risk factors develop preeclampsia in this specific group of oocyte recipients.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 150
Inclusion Criteria
- All major patients with a pregnancy of more than 22 weeks of amenorrhea resulting from an oocyte donation in one of the study centers, having given birth between January 2010 and April 2017 and not opposed to participation in the study.
Exclusion Criteria
- all pregnancies resulting from an oocyte donation abroad, persons of legal age subject to legal protection (safeguard of justice, guardianship, tutorship) and persons deprived of their liberty.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method occurrence of pre-eclampsia through study completion, an average of 1 year
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular biomarkers predict preeclampsia risk in oocyte recipient pregnancies?
How do maternal and donor-derived biomarkers compare in predicting preeclampsia in oocyte recipients?
What are the key pathophysiological mechanisms of preeclampsia in oocyte donation pregnancies?
Are there specific placental biomarkers associated with preeclampsia in gestational carriers?
How does the incidence of preeclampsia in oocyte recipients compare to naturally conceived pregnancies?
Trial Locations
- Locations (2)
CHU de Rennes
🇫🇷Rennes, France
Clinique de la sagesse
🇫🇷Rennes, France
CHU de Rennes🇫🇷Rennes, France