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Preeclampsia clinical trials

View clinical trials related to Preeclampsia.

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NCT ID: NCT02691364 Not yet recruiting - Pregnancy Clinical Trials

Different Regulation of Immune Cells in Patients With Preeclampsia

Start date: April 2016
Phase: N/A
Study type: Observational

Adaptation of the maternal immune system to accommodate the semi-allogeneic fetus is necessary for pregnancy success. Dysregulation of this immune adaptation is implicated in reproductive disorders as infertility, recurrent miscarriage, fetal growth restriction, and preeclampsia. The mechanisms being responsible for fetal tolerance are not known. Several T cell subsets have been implicated in fetal tolerance. The effects of preeclampsia on memory cells are not known. The main objective of this study is to analyze the effect of preeclampsia on levels of immune cells.

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: NCT02633995 Recruiting - Preeclampsia Clinical Trials

Spinal Anaesthesia and Severe Preeclampsia

Start date: December 2015
Phase: N/A
Study type: Observational

The use of spinal anesthesia in pre-eclamptic pregnant woman is of considerable benefit, as these patients present particular hazards with general anaesthesia, such as concerns for rapid airway control and cerebral blood flow alterations during induction of general anaesthesia and intubation However, the incidence of hypotension is high during spinal anesthesia for Cesarean section and it may approach values up to 95 %.

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

NCT ID: NCT02592005 Recruiting - Pregnancy Clinical Trials

Impact of Particulate Matter on Mothers and Babies in Antwerp (IPANEMA)

IPANEMA
Start date: May 2015
Phase: N/A
Study type: Observational

Introduction: An emerging body of evidence indicates that there is an association between air pollution exposure in pregnancy and adverse pregnancy outcomes (Rudra, Williams, Sheppard , Koenig, & Schiff, 2011; Dadvand, et al., 2013; Ritz, et al., 2014). Adverse pregnancy outcomes tend to lead to adverse neonatal outcome and a higher economic cost. Epidemiologic studies have also revealed that cardiovascular complications during pregnancy, such als preeclampsia, are associated with a greater cardiovascular risk during later life ( Abramson & Melvin, 2014). Aim: This study wants to examine the effects of exposure to environmental factors, polluents and particulate matter on the clinical pregnancy outcome for mother and child and to determine which biochemical changes in maternal, placental and cord blood best explain this effect. Methods: This study will be performed in a prospective cohort setup (n=200), recruited from the prenatal clinic in the University Hospital Antwerp. The data collection consists of four questionnaires (intake, both urine samples and postpartum), two blood samples (28 weeks and post-partum), two urine samples (20 and 30 weeks), two hair samples (20 weeks and post-partum), cord blood and the placenta. Results and conclusion: As the study will start in November 2014, no results are available yet.

NCT ID: NCT02558023 Terminated - Hypertension Clinical Trials

The Treatment of Hypertension Associated With Severe Preeclampsia (PE). A Trial of Urapidil Versus Nicardipine

Uranic
Start date: September 2015
Phase: Phase 3
Study type: Interventional

The objective of this study is to demonstrate that urapidil is not inferior to nicardipine for the treatment of hypertension associated with preeclampsia (PE) and that it is better tolerated. - efficacy endpoint : mean arterial blood pressure corrected to 100-120 mmHg after 120 min of study drug administration. - safety endpoints : clinical and biological observation for any side effect. All infants will be observed in the neonatology unit (during 48h). Pharmacokinetic study included to study : - transplacental transfer, - transfer in breast milk, - and neonatal elimination (premature babies of mothers treated with urapidil (less than 33 WG))

NCT ID: NCT02554604 Completed - Preeclampsia Clinical Trials

Identifying HDL Composition and Function in Preeclamptic and Normal Pregnancies

Start date: September 2015
Phase:
Study type: Observational

The study is design to assess if there is a correlation between diagnosis of preeclampsia and its severity to changes in HDL quality, in terms of composition and function and to determine whether preeclampsia-induced changes in VOCs in saliva can be used for the early diagnosis of preeclampsia.

NCT ID: NCT02541110 Not yet recruiting - Preeclampsia Clinical Trials

Prediction of Preeclampsia & Other Obstetric Complications by Serum Homocysteine & Doppler

Start date: September 2015
Phase: N/A
Study type: Observational

Second trimester homocysteine & uterine artery doppler will be assessed& the cases will be followed up till delivery for development of preeclampsia, IUGR(intra-uterine growth retardation) & other obstetric complications.

NCT ID: NCT02527018 Completed - Hypertension Clinical Trials

A Comparison of BNP Levels Using the Nexfin Device in Healthy Pregnant and Preeclamptic Women

Start date: November 2014
Phase: N/A
Study type: Observational

Primary Endpoint: Quantify the hemodynamic changes in preeclampsia using the non-invasive Nexfin device. Secondary Endpoint: Determine if measurable hemodynamic changes are statistically correlated with B-type natriuretic peptide (BNP) levels.