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Pre-eclampsia clinical trials

View clinical trials related to Pre-eclampsia.

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NCT ID: NCT01606774 Completed - Pre-eclampsia Clinical Trials

A Modernized Approach to Prenatal Care in Low Risk Women

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

The investigators plan to identify 80 pregnant women at low risk for obstetrical complications and replace 4-5 routine third trimester visits with a structured program of home weight, blood pressure and urine protein monitoring along with regular structured phone interviews and a 28 week ultrasound. The investigators hypothesis is that this protocol is both safe and acceptable.

NCT ID: NCT01538875 Completed - Clinical trials for Hypertension, Pregnancy Induced

Hydralazine Versus Labetalol for the Management of Hypertensive Disorders of Pregnancy

Start date: July 2012
Phase: Phase 3
Study type: Interventional

Hypertensive crisis (defined as a systolic pressure > 160mmHg or a diastolic pressure > 110mmHg) in patients with a hypertensive disorder of pregnancy is a serious complication with severe and even deadly consequences. The management in this population had been studied, but no consensus has been reached with regards to which treatment is better. Our study will compare two drugs: Hydralazine and Labetalol for the management of hypertensive crisis.

NCT ID: NCT01538147 Completed - Clinical trials for Restless Leg Syndrome

Restless Leg Syndrome and Severe Preeclampsia

Start date: August 1, 2017
Phase: N/A
Study type: Observational

Restless Leg Syndrome is a common but not well recognized central nervous system disorder. It is more prevalent during pregnancy and, if present before pregnancy, can develop an exacerbation of symptoms. In some of the hypothesis trying to explain this syndrome, the physiopathology can also explain hypertensive disorders of pregnancy. So far, no study has been done trying to link both disorders.

NCT ID: NCT01530230 Completed - Preeclampsia Clinical Trials

ST- Depression on Electrocardiogram During Caesarean Section in Regional Anaesthesia in Women With Preeclampsia

Start date: November 2005
Phase: N/A
Study type: Interventional

The investigators examined whether there was a difference in the occurrence of ST depressions after injection of five or ten units of oxytocin, in preeclamptic patients delivered by caesarean section (CS) under regional anesthesia.

NCT ID: NCT01490489 Completed - Pre-eclampsia Clinical Trials

EG-VEGF : Potential Marker of Pre-eclampsia and / or Intrauterine Growth Restriction

EGEVE
Start date: July 11, 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the potential prognostic value of seric concentrations of EG-VEGF for Pre-eclampsia and/or intrauterine growth restriction and will allow checking whether plasma levels of EG-VEGF at 14-18 weeks of gestation could be proposed as prognostic marker for preeclampsia.

NCT ID: NCT01480544 Completed - Sepsis Clinical Trials

Improving Maternal and Child Health in India: Evaluating Demand and Supply Side Strategies (IMATCHINE)

IMATCHINE
Start date: August 2012
Phase: N/A
Study type: Interventional

The study evaluates the impact of a new conditional cash transfer (CCT) program (Thayi Bhagya Yojana) to promote child birth in obstetric facilities in the state of Karnataka, India in order to determine its policy value and to guide efforts to improve maternal and infant health outcomes nationally. In addition, the study includes a large randomized evaluation of performance-based incentive payments to providers to improve quality of medical care provided during delivery and actual health improvement in the providers' patient populations and their catchment areas.

NCT ID: NCT01447290 Completed - Preeclampsia Clinical Trials

Comparison of Random Spot Urine Protein:Creatinine Ratio to 24-Hour Timed Urine Protein Collection in the Evaluation of Preeclampsia

P:C Ratio
Start date: May 2012
Phase: N/A
Study type: Observational

This is a non-inferiority, prospective study of the relationship between the 24-hour urine protein collection and spot protein:creatinine ratio in the diagnosis of preeclampsia involving a sample of 18-45 year-old pregnant women attending the new Obstetrics orientation. The investigators will follow all participants who consent to be part of this study throughout their entire pregnancy. Those who get evaluated for preeclampsia will then have a P:C ratio anytime their Primary Obstetrics provider orders a standard of care 24-hour urine collection (standard of care). Those participants who are not evaluated for preeclampsia during their pregnancy will be dropped from the study. Participants evaluated for preeclampsia during the prenatal period will be asked to provide a random spot clean-catch urine sample at intervals of approximately 0 and 24 hours following the initiation of the 24-hour urine collection. The patient's demographic and clinical data, as well as the spot protein:creatinine ratio and 24-hour urine protein will be collected and analyzed at the conclusion of the study period.

NCT ID: NCT01431443 Completed - Preeclampsia Clinical Trials

Consumption of Chocolate in Pregnant Women.

CHOCENTA
Start date: May 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate the acute and chronic effect of consumption of flavanol-rich chocolate on endothelium function in pregnant women at high risk for preeclampsia.

NCT ID: NCT01408979 Completed - Severe Preeclampsia Clinical Trials

Effectiveness Study of Short Course of Magnesium Sulfate for Severe Preeclamsia

MgSO4
Start date: August 2011
Phase: Phase 4
Study type: Interventional

Magnesium sulfate is the ideal drug for seizures prophilaxis in preeclampsia. The ideal duration of this treatment after delivery is still to be established. The hypothesis is that in stable patients a shorter course of treatment is possible without prejudice to the mother.

NCT ID: NCT01404910 Completed - Preeclampsia Clinical Trials

Removal of Anti-Angiogenic Proteins in Preeclampsia Before Delivery

RAAPID-II
Start date: May 2013
Phase: N/A
Study type: Interventional

Preeclampsia is a syndrome that occurs in approximately 3% to 8% of pregnancies and is associated with considerable maternal and neonatal morbidity and mortality. Except for termination of the pregnancy, effective treatments/preventative measures for preeclampsia are lacking. Although prolongation of pregnancy benefits the fetus, it is detrimental to the mother, and is associated with hypertension, proteinuria, and symptoms that suggest kidney, brain, liver and cardiovascular system involvement. Placental soluble fms-like tyrosine kinase 1 (sFlt-1) is elevated in women with preeclampsia, with levels that fall after delivery. sFlt-1 is a variant of the vascular endothelial growth factor (VEGF) receptor Flt-1, and in the circulation, acts as a potent VEGF and placental growth factor (PlGF) antagonist. Given that sFlt-1 levels are elevated in preeclampsia, we are investigating if removal of sFlt-1 from the plasma of women with preeclampsia can improve maternal and fetal outcomes. Short-term extracorporeal apheresis with the LIPOSORBER LA-15 System will be the primary intervention using methods that have been previously applied in pregnant women with familial hypercholesterolemia.