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Pre-eclampsia clinical trials

View clinical trials related to Pre-eclampsia.

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NCT ID: NCT02704676 Not yet recruiting - Pre-Eclampsia Clinical Trials

CA-125 and Severity of Pre-Eclampsia

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

The Aim of this study is to determine the relationship between serum concentrations of cancer antigen-125 (CA-125) and pre-eclampsia severity.

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: 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: NCT02314286 Not yet recruiting - Clinical trials for Severe Pre-eclampsia

Rosuvastatin in Order to Induce Preeclampsia Resolution in Severe PET up to 48 Hours Following Delivery

Start date: December 2014
Phase: Phase 1/Phase 2
Study type: Interventional

Prospective randomized single blind trial. Study population are women diagnosed with severe pre-eclampsia during singleton pregnancy, between 24+0 weeks and 41+6 weeks gestational age. The purpose of the study is to evaluate the effect of Rosuvastatin on the severe preeclampsia resolution at 48 hours after delivery. After screening and signing an informed consent form, before entering delivery room, a randomization 1:1 will be carried. 50 women will be in the treatment arm while 50 will be in the control arm. Both groups will be treated according to ACOG (The American College of Obstetricians and Gynecologists has the following clinical guidelines related to deliveries before 39 weeks) guidelines. In addition, following randomization experimental group will be treated with Rosuvastatin 40mg that will be administrated orally with or without food. Treatment will be carried within the first hour following delivery. Another dose will be given 24 hours after first administration. Control group will be treated with placebo.

NCT ID: NCT02045316 Not yet recruiting - Preeclampsia Clinical Trials

The Expression of Aquaporin 3, 8 and 9 in Placenta in Normal and Preeclamptic Pregnancies: Perinatal and Neonatal Outcomes.

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

The etiologic agent responsible for the development of preeclampsia remains unknown. Aquaporins, members of integral membrane proteins, are responsible of water molecules movements through the plasma membrane channels, energy metabolism and associated with changes in cellular volume during apoptosis. İn such placental pathology as preeclampsia, characterized with superficial implantation and increased apoptosis leading to a relative hypoxia between mother and fetus, the hypothesis of aquaporins important role in energy homeostasis and apoptosis maybe suggested.

NCT ID: NCT02007837 Not yet recruiting - Clinical trials for Pregnancy Induced Hypertension

Prospects for the Prevention of Pregnancy-induced Hypertension and Preeclampsia Trial

4P
Start date: January 2018
Phase: Phase 3
Study type: Interventional

Hypertensive disorders of pregnancy (HDP) are with 50.000 deaths every year one of the major causes of maternal mortality worldwide, especially in low and middle income countries. This trial aims to determine whether a daily dose of combined low-dose aspirin, calcium, vitamin D3, folic acid and vitamin B12 in pregnancy reduces the incidence of pregnancy-induced hypertension in women at risk. Secondary and tertiary objectives include other maternal and neonatal outcomes.

NCT ID: NCT01890005 Not yet recruiting - Preeclampsia Clinical Trials

Low Dose Aspirin for the Prevention of Preeclampsia

Start date: July 2013
Phase: Phase 3
Study type: Interventional

Preeclampsia is one of the three leading causes of maternal morbidity and mortality all over the world. The use of low dose aspirin has been mentioned in several studies with promising results. The investigators decided to evaluate the use of low dose aspirin, starting between 13 and 16 weeks of pregnancy, based on clinical characteristics only to reduce the incidence of preeclampsia.

NCT ID: NCT01804751 Not yet recruiting - Preeclampsia Clinical Trials

Prediction of Adverse Perinatal Outcome for Preeclampsia in Sichuan Province of China

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

The purpose of this study is to build a model for the prediction of adverse perinatal outcome for preeclampsia in china

NCT ID: NCT01538121 Not yet recruiting - Clinical trials for Antiphospholipid Syndrome

Antiphospholipid Antibodies and Early Severe Preeclampsia.

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

The Antiphospholipid Syndrome is an immune disease where the presence of antibodies directed against cell membrane phospholipids (antiphospholipid antibodies) can cause an hypercoagulable state that causes thrombosis and obstetric complications (miscarriages, stillbirths). Since 1999 the Sapporo Criteria for Antiphospholipid Syndrome diagnosis includes the development of severe preeclampsia before 34 weeks of gestation, but this was done without solid evidence of a relation between the two. Our study will try to add information to this particular point.

NCT ID: NCT00928213 Not yet recruiting - Preeclampsia Clinical Trials

PP13 and Doppler Study to Predict Preeclampsia

Start date: August 2009
Phase: Phase 2/Phase 3
Study type: Interventional

Assessment of biochemical and sonographic marker to predict the risk for developing preeclampsia Among biochemical markers are serum level of Placental Protein 13 (PP13) and Placenta Growth factor (PIGF). For sonographic marker Doppler pulsatility Index of the blood flow through the uterine maternal arteries is assessed. PP13 is produced by the placenta and released to the maternal blood circulation. It has been shown to be an effective serum marker for early onset preeclampsia (Nicolaides KH et al., 2005). The purpose of this study is to combined the assessment of the biochemical markers with Doppler in the first and the second trimester to provide a comprehensive evaluation of various methods for sequential and combined analysis to assess the risk for developing preeclampsia.