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Eclampsia clinical trials

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NCT ID: NCT00175695 Completed - Pre-eclampsia Clinical Trials

Disease Modification in Toxaemia of Pregnancy

Start date: December 2004
Phase: Phase 2
Study type: Observational

Short description of the primary purpose of the protocol intended for the lay public. Include brief statement of study hypothesis Pre-eclampsia (toxemia of pregnancy) is the most cause of death among pregnant women in North America. It also causes many complications for fetuses (unborn children) and neonates (newborn children). Pre-eclampsia is defined by high blood pressure (hypertension), the loss of protein into the urine (proteinuria), and disorders of many body systems, including the blood clotting (coagulation) and inflammation. What is needed is a compound that will safely prolong pregnancies, to give babies more time to grow inside their mothers, and will help the recovery in those mothers after delivery. We are going to investigate a compound (recombinant human activated protein C (rhAPC)) that has the potential to modify disease activity in pre-eclampsia by reducing coagulation and inflammation disorders. rhAPC is effective in patients suffering from septic shock. We will test rhAPC in women who develop severe pre-eclampsia in two ways. First, in women with severe pre-eclampsia remote from term who are carrying small babies (intent: safely prolong their pregnancies). Second, in women who have had severe pre-eclampsia before their baby delivered (including women in the first group), or whose disease develops/worsens after delivery (intent: switch off the disease so dangerous complications do not arise). This study is a preliminary one to look for possible risks and benefits for these women. Only 40 women will be studied to provide initial evidence on which to base a larger international trial which is planned. We will study their pregnancy outcomes as well as markers of disease activity, to gain a better understanding of the mechanisms by which these women become unwell.

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: NCT00141310 Terminated - Pre-eclampsia Clinical Trials

Sildenafil Citrate for the Treatment of Established Pre-Eclampsia

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

To determine the efficacy and safety of sildenafil citrate in the treatment of established pre-eclampsia

NCT ID: NCT00133926 Unknown status - Clinical trials for Periodontal Diseases

Prevention of Pre-Term Birth by Treatment of Periodontal Disease

Start date: March 2005
Phase: Phase 2
Study type: Interventional

The aim of the study is to investigate, in an Australian population of pregnant women, whether the treatment of periodontal disease during pregnancy prevents pre-term birth and other complications of pregnancy. Dental screening and periodontal treatment protocols have been based on standard techniques employed by hygienists that can be readily applied to the general obstetric population.

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: 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: NCT00000534 Completed - Hypertension Clinical Trials

Calcium for Pre-Eclampsia Prevention (CPEP)

Start date: March 1991
Phase: Phase 3
Study type: Interventional

To evaluate the efficacy of 2 grams per day of oral calcium supplementation in reducing the combined incidence of hypertensive disorders of pregnancy: pre-eclampsia, eclampsia, and the HELLP Syndrome (hypertension, thrombocytopenia, hemolysis, and abnormal liver function). The National Institute of Child Health and Human Development (NICHD) initiated the trial in 1991, with joint funding provided by the National Heart, Lung, and Blood Institute in fiscal years 1992, 1993, and 1995.