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Pre-eclampsia clinical trials

View clinical trials related to Pre-eclampsia.

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NCT ID: NCT01278459 Completed - Pre-Eclampsia Clinical Trials

Can Atorvastatin Improve Vascular Function in Women With a History of Preeclampsia?

PVS3
Start date: October 2011
Phase: Phase 3
Study type: Interventional

The purpose of the study is to test the hypothesis that a short course of atorvastatin can improve vascular function in women with a history of preeclampsia, compared to placebo.

NCT ID: NCT01261884 Completed - Hypertension Clinical Trials

Exercise in Pregnancy for Reduction of Blood Pressure in Obese Patients

Start date: November 2010
Phase: N/A
Study type: Interventional

Preeclampsia and other high blood pressure disorders of pregnancy are a significant cause of both maternal and fetal complications of pregnancy. To date, there is no known "cure" for preeclampsia, but studies have shown that exercise may lower the risk of preeclampsia and high blood pressure disorders in pregnancy. Resistance training also lowers blood pressure, and may be easier to perform in a pregnant population, leading to higher compliance. The investigators propose to perform a novel prospective study of a resistance training regimen on blood pressure in pregnant patients at high risk for developing preeclampsia or high blood pressure.

NCT ID: NCT01261351 Completed - Pre Eclampsia Clinical Trials

Study of Coagulation Activation Markers and Pre Eclampsia

PRESTIGE
Start date: May 2010
Phase: N/A
Study type: Observational

The primary purpose of the trial is to evaluate coagulation activator markers in patients with pre eclampsia compared to control (normal pregnancy) and to correlate these markers with the severity of the pathology.

NCT ID: NCT01255202 Recruiting - Clinical trials for Preeclampsia/Toxemia

The Prediction of Preeclampsia/Toxemia in Twin Pregnancy

Start date: September 2009
Phase: N/A
Study type: Observational

The purpose of this study is to finout whetere uterinae artery flow , PP13 and endogolin levels in the serum and kongo red in the urine can predict preeclamsia toxemia in twin pregnancies.

NCT ID: NCT01248169 Completed - Clinical trials for Pregnancy; Hypertension, Gestational Hypertension, With Albuminuria (Severe Pre-eclampsia)

Impedance Cardiographic (ICG) Assessment of Pregnant Women With Severe Hypertension to Assess Impact of Standard Therapy

ICASH
Start date: December 2009
Phase: N/A
Study type: Observational

The utilization of external cardiohemodynamic patient assessment, applying non-invasive stick-on contact patches to the mother's neck on either side and chest wall on either side, enables the practitioner to have information about the patient's cardiac function and vascular status beyond simply blood pressure and pulse. This information, once collected, should open the practitioner's eyes to better assess the patient's disease status and her response to therapy. We will use this information to compare the effectiveness of the two standard medications used for treatment of maternal high blood pressure.

NCT ID: NCT01232205 Completed - Preeclampsia Clinical Trials

Antioxidant Supplementation in Pregnant Women

ASIP1
Start date: June 2001
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to investigate the benefit of several micro nutrients of antioxidants (using milk) in a cohort of women with low antioxidant status and the changes in cell-free mRNA.

NCT ID: NCT01229189 Completed - Clinical trials for Vitamin D Deficiency

Evaluation of the Effectiveness of Vitamin D Supplementation to Pregnant Women and Their Infants in Pakistan.

Start date: February 2010
Phase: N/A
Study type: Interventional

Vitamin D deficiency is wide spread in South Asian population and is contributing to burden of disease in this region including Pakistan. The relative importance of vitamin D deficiency, mutation in its receptor and maternal and child health has not been established in Pakistan and population based studies are required to explore and avert the maternal and Neonatal complications and consequences of Vitamin D deficiency The trial will evaluate the effectiveness of Vitamin D supplementation to pregnant women and their Infants. It will be a double blind placebo controlled trial, which will be conducted in a rural district of Pakistan.

NCT ID: NCT01195441 Completed - Preeclampsia Clinical Trials

Prediction and Prevention of Preeclampsia by First Trimester Ultrasound

Screen-tox
Start date: September 2010
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether the Fetal Medicine Foundation algorithm for individual risk calculation for preeclampsia (PE) and pregnancy induced hypertension (PIH) is suitable to identify women in high risk of developing these diseases in a Norwegian population.

NCT ID: NCT01193192 Terminated - Pre-eclampsia Clinical Trials

A Retrospective Analysis of Neevo® and NeevoDHA® Compared to a Standard Prenatal Vitamin in Anemia During Pregnancy

Start date: July 2010
Phase: N/A
Study type: Observational

This study is a multi-site, retrospective chart review to determine the effect of Neevo® or NeevoDHA® (with higher folate and B12) versus standard prenatal vitamins on hemoglobin (Hgb) levels in pregnant women throughout the course of pregnancy. Neevo® is a prescription medical food indicated for the dietary management of women under a doctor's care who face high risk pregnancies, older overactive bladder (OB) patients and patients unable to fully metabolize folic acid. Data will be collected from existing patient charts of subjects administered Neevo® or NeevoDHA® daily compared to subjects administered a prenatal vitamin daily.

NCT ID: NCT01192412 Completed - Clinical trials for Gestational Hypertension

The CHIPS Trial (Control of Hypertension In Pregnancy Study)

Start date: April 2009
Phase: N/A
Study type: Interventional

The investigators do not know which approach to treatment of non-severe high blood pressure in pregnancy is better for women and babies. In the CHIPS Trial, the investigators seek to determine whether 'less tight' control (aiming for a diastolic blood pressure [dBP] of 100 mmHg), compared with 'tight' control (aiming for a diastolic blood pressure [dBP] of 85 mmHg) can decrease the risks of adverse baby outcomes without increasing the risk of problems for the mother.