sFlt1/PlGF and Planned Delivery to Prevent Preeclampsia at Term.
Recruiting
N/A
Interventional Study
Preeclampsia
Intrauterine Growth Restriction
Maternal Hypertension
Neonatal Outcome
Perinatal Death
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.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 9,132 (estimated)
- Sponsor
- Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau · Other
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About This Trial
* Preeclampsia (PE) affects \~5% of pregnancies. Although improved obstetrical care has significantly diminished associated maternal mortality, PE remains a leading cause of maternal morbidity and mortality in the world.
* Term PE accounts for 70% of all PE and a large proportion of maternal-fetal morbidity related with this condition. Prediction and prevention of term PE remains unsolved.
* Previ…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Nulliparous women
* Singleton pregnancies
* \>18 years old
* 35.0-36.6 weeks of gestation
* Maternal written consent form
Exclusion Criteria:
* Fetuses/neonates with major malformations or genetic anomalies that could modify the timing of delivery or has an impact on obstetr…
Contacts