NOPE37: Angiogenic Factors for Managing Term Preeclampsia

Recruiting N/A Interventional Study
Preeclampsia
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Female
Study type
Interventional
Purpose
Treatment
Participants needed
750 (estimated)
Sponsor
Hospital Universitari Vall d'Hebron Research Institute · Other
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About This Trial

This study tests the hypothesis that, in women with preeclampsia without severe features, delivery management based on sFlt-1/PlGF would reduce the rate of induction of labor without worsening the rate of progression to preeclampsia with severe features and other maternal complications.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age ≥18 years * Singleton pregnancy * Preeclampsia without severe features according to the ACOG definition * Antegrade diastolic flow in the umbilical artery Doppler * Gestational age between 36+0 and 38+6 weeks of gestation * Gestational age confirmed by fetal crown-rump len…
Contacts

Erika Bonacina, MD, PhD

003493 489 30 00

erika.bonacina@vallhebron.cat

CONTACT