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Preeclampsia clinical trials

View clinical trials related to Preeclampsia.

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NCT ID: NCT02791568 Completed - Obesity Clinical Trials

Advanced MRI for Uteroplacental Flow, Perfusion, Oxygenation & Inflammation

Start date: January 31, 2017
Phase:
Study type: Observational

The purpose of the study is to develop advanced ultrasound (U/S) and Magnetic Resonance Imaging, known as MRI to study uteroplacental health. The goal of this study is to evaluate the blood and oxygen flow to the placenta using advanced U/S and MRI testing.

NCT ID: NCT02780414 Completed - Hypertension Clinical Trials

Collection of Samples From Pregnant Women for the Evaluation of Preeclampsia (Pre-E) Biomarkers

Start date: January 2016
Phase:
Study type: Observational

Preeclampsia (Pre-E) is a hypertensive disease of pregnancy with multi-system involvement that usually occurs in the second half of pregnancy. Pre-E occurs in 5% to 7% of U.S. pregnancies, and is the third-leading cause of U.S. maternal death. Improvements to the current diagnostic paradigm have been evaluated. However, no stand-alone diagnostic method has emerged that more accurately identifies women at risk for preeclampsia, warranting improvements in diagnosing Pre-E. This sample collection study will obtain serum and urine samples from pregnant women who present with clinical signs, symptoms, or conditions contributing to the suspicion of Pre-E. Samples will be used to evaluate and validate the performance of an assay intended to aid in assessing the risk of Pre-E.

NCT ID: NCT02765906 Completed - Hypertension Clinical Trials

Comparing Different Methods of Patient Education on Preeclampsia

Start date: May 2016
Phase: N/A
Study type: Interventional

Preeclampsia is a life-threatening condition unique to pregnancy which occurs in 5-8% of all pregnancies. It contributes to a large proportion of maternal mortality worldwide and these deaths largely result from delayed diagnosis. A number of studies have shown that patient knowledge about preeclampsia is poor and that patient education can improve patient awareness. The investigators would like to find out what type of patient education is most effective. The investigators propose a three arm randomized controlled trial (RCT) where the first arm will receive a graphic card depicting signs and symptoms of preeclampsia, the second arm will watch an educational video on preeclampsia, and the third arm will have no visual form of patient education; they will be exposed only to the counseling they receive with their routine prenatal care. The card and video were both developed by the Preeclampsia Foundation and in a prior RCT the card was shown to be a useful educational intervention. This study would expand on this previous data by comparing the graphic card to an informational video available on the Preeclampsia Foundation's website (http://www.preeclampsia.org/component/allvideoshare/video/featured/7-symptoms-every-pregnant -woman-should-know?Itemid=479). The effectiveness of this video has not yet been tested as an educational tool. Patients in the arm receiving the graphic card for educational intervention will be allowed to keep this card. Primiparous patients seen in the ambulatory prenatal clinic and Maternal Fetal Medicine (MFM) clinic will be enrolled at 18w0d-24w6d gestation. At the time of enrollment baseline preeclampsia knowledge, demographics, and patient anxiety before and after initial exposure to the educational interventions will be assessed. A follow up assessment of knowledge of preeclampsia will be obtained at 32-36 weeks gestation to measure retention of knowledge. Patient medical records will be reviewed for delivery outcomes which will be recorded and compared.

NCT ID: NCT02754778 Completed - Preeclampsia Clinical Trials

Influence of Conditional Workout Postpartum on Arterial Stiffness Among Women With Status After Preeclampsia, Superimposed Preeclampsia or HELLP-syndrome

RedCarRisk
Start date: April 2016
Phase: N/A
Study type: Interventional

Evaluation of practicability in survey and test procedures and of successful implementation of complex interventions - feasibility analysis based on a pilot study: Influence of conditional workout postpartum on arterial stiffness among women with status after preeclampsia, superimposed preeclampsia or HELLP-syndrome

NCT ID: NCT02699827 Completed - Preeclampsia Clinical Trials

Adding MgSO4 to Epidural Levobupivacaine in CS for Patients With Preeclampsia

Start date: March 2016
Phase: Phase 4
Study type: Interventional

This study aims at evaluating the effect of adding magnesium sulphate epidurally as an adjunct to levobupivacaine on the quality of anesthesia and perioperative pain relief in patients with preeclampsia undergoing elective caesarian section (CS).

NCT ID: NCT02699437 Completed - Preeclampsia Clinical Trials

Prevalence of Antiphospholipid Antibodies Among Women With Preeclampsia

Start date: January 1, 2017
Phase:
Study type: Observational

The purpose of this study is to determine the prevalence of positive antiphospholipid antibodies among women with preeclampsia and to determine the effect of antiphospholipid antibodies on the severity of preeclampsia and the obstetric outcomes

NCT ID: NCT02693041 Completed - Preterm Birth Clinical Trials

Pregnancy Complications - A Probiotic Interventional Study

Start date: June 2012
Phase: N/A
Study type: Interventional

Investigators hypothesize that a) probiotics decrease the overall inflammatory state in the pregnant woman, especially in women with high risk pregnancies.

NCT ID: NCT02639676 Completed - Preeclampsia Clinical Trials

Anti-Angiogenic Preeclampsia Milieu Impairs Infant Lung and Vascular Development

Start date: February 11, 2016
Phase:
Study type: Observational

Pregnant mothers who develop high blood pressure and other vascular problems (preeclampsia) deliver babies with increased neonatal health problems, which include lung disease and vascular complications, later in life. Investigators will evaluate whether infants of mothers with preeclampsia have evidence for impaired development of the lungs and blood vessels.

NCT ID: NCT02611011 Completed - Preeclampsia Clinical Trials

Assessing the Usability and Clinical Utility of the Congo Red Dot Test: A Survey

Start date: March 1, 2018
Phase:
Study type: Observational

To determine if women can understand the instructions, carry out the test, and interpret the test results. Women will be recruited to complete a test instruction and comprehension assessment and a usability assessment.

NCT ID: NCT02610972 Completed - Preeclampsia Clinical Trials

Assessing the Usability and Clinical Utility of the Congo Red Dot Test: A Case-control Study

Start date: December 1, 2018
Phase:
Study type: Observational

A case-control study will evaluate the clinical utility of the Congo Red test GV-005 in following women with a clinical diagnosis of preeclampsia and clinically healthy women in the postpartum period