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Severe Preeclampsia clinical trials

View clinical trials related to Severe Preeclampsia.

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NCT ID: NCT04058405 Completed - Severe Preeclampsia Clinical Trials

Risk Prediction Models for Adverse Maternal and Neonatal Outcomes in Preeclampsia

Start date: November 12, 2018
Phase:
Study type: Observational

This proposal describes a single centre retrospective cross-sectional study which will address the need to further develop and test statistical risk prediction models for adverse maternal and neonatal outcomes in low-resource settings; this will be the first such research to be carried out in Zimbabwe.

NCT ID: NCT03164304 Completed - Severe Preeclampsia Clinical Trials

Efficacy and Safety of 1 g Vs 2 g Per Hour Intravenous Maintenance Dose of MgSO4 in Women With Severe Pre-eclampsia

Start date: May 30, 2017
Phase: Phase 4
Study type: Interventional

Preeclampsia is commonly viewed as one of the hypertensive pregnancy disorders, which cover a spectrum of clinical presentations from chronic hypertension ( hypertension occurring prior to 20 weeks of gestation) and gestational hypertension (hypertension occurring after 20 weeks of gestation) To more severe forms, including preeclampsia, eclampsia (its convulsive form), and HELLP syndrome (hemolysis, elevated liver enzyme S, and low platelets)

NCT ID: NCT02379832 Completed - Preterm Birth Clinical Trials

Pre-Eclampsia And Growth Restriction: a Longitudinal Study

PEARL
Start date: March 2015
Phase:
Study type: Observational [Patient Registry]

Preeclampsia may have several causes leading to different characteristics of the pathology. Differentiation between the "type of preeclampsia" would help to treat patients more accurately. This project aims to identify early markers that are specific to each type of preeclampsia (early or late, with or without growth restriction). Through a case-control study, many data will be collected prospectively (serum markers, ultrasonographic markers, maternal factors) among nulliparous women with no sign of preeclampsia (as soon as the first trimester) and nulliparous women with preeclampsia (at diagnosis).

NCT ID: NCT02189148 Completed - Preterm Birth Clinical Trials

First-trimester Prediction of Preeclampsia

PREDICTION
Start date: November 2014
Phase:
Study type: Observational

Preeclampsia is a complication of pregnancy related to adverse maternal and neonatal outcomes, including fetal growth restriction and perinatal death. Several measures are used or under investigation (low-dose aspirin, low-molecular weight heparin, calcium, folic acid, among others) for the prevention of preeclampsia. Unfortunately, most high-risk women who could benefit from those preventive measures are not identified until late in pregnancy. Recent evidences suggest that the investigators could identify women at risk of developing preeclampsia using a combination of serum and ultrasound biomarkers in the first-trimester of pregnancy. This screening test needs external validation. A first-trimester screening strategy will strengthen clinical research on preeclampsia and will contribute to the development of strategy combining the prediction and prevention of the disease and its related complications.

NCT ID: NCT01538147 Completed - Clinical trials for Restless Leg Syndrome

Restless Leg Syndrome and Severe Preeclampsia

Start date: August 1, 2017
Phase: N/A
Study type: Observational

Restless Leg Syndrome is a common but not well recognized central nervous system disorder. It is more prevalent during pregnancy and, if present before pregnancy, can develop an exacerbation of symptoms. In some of the hypothesis trying to explain this syndrome, the physiopathology can also explain hypertensive disorders of pregnancy. So far, no study has been done trying to link both disorders.

NCT ID: NCT01408979 Completed - Severe Preeclampsia Clinical Trials

Effectiveness Study of Short Course of Magnesium Sulfate for Severe Preeclamsia

MgSO4
Start date: August 2011
Phase: Phase 4
Study type: Interventional

Magnesium sulfate is the ideal drug for seizures prophilaxis in preeclampsia. The ideal duration of this treatment after delivery is still to be established. The hypothesis is that in stable patients a shorter course of treatment is possible without prejudice to the mother.