Eclampsia Preeclampsia

2

Review clinical trials related to Eclampsia Preeclampsia. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Modelization of Early Endometrial-trophoblast Molecular Interaction

Despite significant advances in assisted reproductive technology, only 25% of in vitro fertilization (IVF) embryo transfers result in pregnancy, largely due to implantation failure. Preeclampsia complicates 2 to 5% of pregnancies, causes 76,000 maternal deaths worldwide each year, and is one of the leading causes of extreme prematurity (20% of premature births occurring before 32 weeks of gestation). The MEETMI project aims to characterize, in the laboratory, the early endometrium-trophoblast molecular interactions that determine the initial stages of human implantation and placentation. As part of routine care, patients will undergo a diagnostic hysteroscopy during which a endometrial biopsy may be performed. If the patient consents to participate in the study, an additional extended endometrial biopsy will be collected for research purposes.

Participants needed: 500
Trial details
Age: 18-50Biological sex: FemaleType: InterventionalSponsor: Centre Hospitalier Intercommunal CreteilUpdated: Sep 17, 2026Locations: 1
Eligibility criteria

Medical indication for a diagnostic hysteroscopy between the ages of 18 and 50 [+2]

Current pregnancy [+8]

Status: Not yet recruiting

Levetiracetam Compared to Magnesium Sulfate for Prevention of Eclamptic Seizure

The goal of this study is to compare levetiracetam to magnesium sulfate for the prevention of eclamptic seizures in pregnant persons with severe preeclampsia that are 32 or more weeks pregnant. This is an equivalence study so our primary goal is to see no difference in the incidence of seizure in the two groups. Since side effects can be a significant problem with magnesium sulfate and these patients are at significant risk of life threatening complications, we also plan to evaluate several secondary outcomes in the mothers and the babies, including: severe allergic reaction, magnesium toxicity, ICU admission, hospital readmission, transfusion for any reason, pulmonary edema, cardiomyopathy, Posterior Reversible Encephalopathy Syndrome, eclamptic seizure, loss of vision, stroke, renal injury requiring dialysis, cardiac arrest, maternal death, unexpected stillbirth or neonatal death, NICU admission, Apgars and length of neonatal respiratory support.

Participants needed: 1,240
Trial details
Phase: Phase 3Age: 19+Biological sex: FemaleType: InterventionalSponsor: Nebraska Methodist Health SystemUpdated: Oct 24, 2025Locations: 1
Eligibility criteria

Pregnant or postpartum women aged 19 years or older [+4]

<32 weeks estimated gestational age [+4]