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Pre-eclampsia clinical trials

View clinical trials related to Pre-eclampsia.

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NCT ID: NCT00158743 Completed - Pre-eclampsia Clinical Trials

Efficacy Study of Digibind for Treatment of Severe Preeclampsia

Start date: February 2004
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether a commercially available anti-digoxin antibody, Digibind, can delay delivery in patients with severe pre-eclampsia. If so, this would allow more time for maternally administered steroids to prevent the development of respiratory complications in premature infants.

NCT ID: NCT00157521 Completed - Pre-Eclampsia Clinical Trials

L-Arginine in Pre-Eclampsia

Start date: September 2002
Phase: Phase 3
Study type: Interventional

Pre-eclampsia is a disorder unique to pregnancy affecting both the mother and the fetus. Hypertension, proteinuria and edema are the most common and well-known maternal clinical symptoms. The incidence is approximately 6-8%. Pre-eclampsia is one of the leading causes of maternal and fetal mortality and morbidity associated with pregnancy throughout the world. The pathophysiology is unknown. At present, the most effective treatment is immediate delivery. The researchers' studies contributed to the demonstration that the vasodilator nitric oxide (NO) is important for correct placentation and that less nitric oxide (NO)- dependent vasodilation and an excess formation of reactive oxygen species explain poor placenta perfusion in pre-eclampsia. This reduced NO activity and increased oxidative stress in pre-eclamptic placenta is related to low bioavailability of L-arginine, the NO precursor. In this pilot study the researchers want to evaluate whether the administration of L-arginine to women with a clinical diagnosis of preeclampsia might restore physiological NO production in the placenta and ameliorate the pregnancy outcome.

NCT ID: NCT00135707 Completed - Preeclampsia Clinical Trials

Combined Antioxidant and Preeclampsia Prediction Studies (CAPPS)

CAPPS
Start date: June 2003
Phase: Phase 3
Study type: Interventional

Preeclampsia is one of the most common complications of pregnancy and is characterized by high blood pressure and protein in the urine. This can cause problems in the second half of pregnancy for both the mother and fetus. This study of preeclampsia consists of two parts: 1) a randomized, placebo controlled, multicenter clinical trial of 10,000 low-risk nulliparous women between 9 and 16 weeks gestation and 2) an observational, cohort study of 4,000 patients between 9 and 12 weeks gestation who are also enrolled in the trial. Subjects in both parts will receive either 1000 mg of vitamin C and 400 IU of vitamin E or matching placebo daily. The purpose of the randomized, clinical trial is to find out if high doses of vitamin C and E will reduce the risk of preeclampsia and other problems associated with the disease. The study will also evaluate the safety of antioxidant therapy for mother and infant. Patients will be seen monthly to receive their supply of study drug, to have weight and blood pressure recorded, to have urine protein measured, and to assess any side effects. At two visits, blood and urine will be collected. The observational, cohort study will prospectively measure potential biochemical and biophysical markers that might predict preeclampsia. These patients will have additional procedures including uterine artery Doppler and blood drawn for a complete blood count (CBC).

NCT ID: NCT00097110 Completed - Pregnancy Clinical Trials

RCT of Antioxidant Therapy to Prevent Preeclampsia in Brazil

Start date: July 2003
Phase: Phase 3
Study type: Interventional

The perinatal morbidity and mortality rates for Brazil are five to ten-fold higher than those reported for upper income countries. This study tests the likelihood that the joint administration of antioxidants vitamin C (1000 mg) and vitamin E (400 IU) will reduce the incidence of preeclampsia among chronically hypertensive pregnant patients and patients with a past history of preeclampsia/eclampsia.

NCT ID: NCT00005456 Completed - Hypertension Clinical Trials

Hypertensive and Normal Pregnancy--Calcium Metabolism and Renin-Angiotensin - SCOR in Hypertension

Start date: December 1990
Phase: N/A
Study type: Observational

To study calcium metabolism and the renin-angiotensin system in hypertensive and normal pregnancy.

NCT ID: NCT00005400 Completed - Clinical trials for Cardiovascular Diseases

Angiotensinogen Variants and Adverse Pregnancy Outcomes

Start date: August 1995
Phase: N/A
Study type: Observational

To examine angiotensinogen genetic variants and adverse pregnancy outcomes.

NCT ID: NCT00005208 Completed - Hypertension Clinical Trials

Regulation of Placental Vascular Reactivity in Pregnancy-induced Hypertension

Start date: September 1987
Phase: N/A
Study type: Observational

To elucidate the role of an imbalance in vasodilator prostacyclin (PGI2) and vasoconstrictor thromboxane (TxA2) in pregnancy-induced hypertension

NCT ID: NCT00005207 Completed - Hypertension Clinical Trials

Renin and Prorenin in Pregnancy

Start date: September 1987
Phase: N/A
Study type: Observational

To determine the role of the prorenin-renin-angiotensin-aldosterone system (RAAS) in normal and hypertensive pregnancy.

NCT ID: NCT00004399 Completed - Pre-eclampsia Clinical Trials

Randomized Study of Nimodipine Versus Magnesium Sulfate in the Prevention of Eclamptic Seizures in Patients With Severe Preeclampsia

Start date: September 1995
Phase: N/A
Study type: Interventional

OBJECTIVES: I. Determine the effectiveness of nimodipine versus magnesium sulfate in the prevention of eclamptic seizures in patients with severe preeclampsia.

NCT ID: NCT00000543 Completed - Hypertension Clinical Trials

Oral Calcium in Pregnant Women With Hypertension

Start date: August 1993
Phase: Phase 2
Study type: Interventional

To determine of providing calcium supplementation to women with pre-existing hypertension reduces the level of blood pressure, requirement for antihypertensive drugs, and incidence of pre-eclampsia.