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Pre-eclampsia clinical trials

View clinical trials related to Pre-eclampsia.

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NCT ID: NCT03668184 Completed - Pregnancy Clinical Trials

What Are the Predictive Factors for Preeclampsia in Oocyte Recipients? - PREROVE

PREROVE
Start date: January 2, 2018
Phase:
Study type: Observational

The main goal is to determine which risk factors develop preeclampsia in this specific group of oocyte recipients.

NCT ID: NCT03665623 Completed - Pre-Eclampsia Clinical Trials

Prediction of Preeclampsia by Comprehensive Markers.

Start date: December 1, 2017
Phase:
Study type: Observational

Preeclampsia is one of the most serious complications in pregnancy that causes maternal death and preterm delivery. Series studies has show that the competing risk model developed by the Fetal Maternal FouNdation in early pregnancy has the potential to predict preeclampsia effectively but has show crowd difference. We aim to evaluate the performance of various screening model based on FMF model in Chinese population.

NCT ID: NCT03661775 Completed - Clinical trials for Severe Pre-eclampsia

Serum Magnesium Level Administration in Severe Pre-eclampsia Obese Pregnancy

Start date: September 30, 2018
Phase: N/A
Study type: Interventional

Comparison of the magnesium level in difference continuous rate in women who were diagnosed severe pre-eclampsia obese

NCT ID: NCT03650790 Completed - Pre-Eclampsia Clinical Trials

C1q/TNF-related Protein 9 (CTRP 9) Level in Preeclamptic Obese and Non-obese Pregnancies

CTRP
Start date: September 3, 2018
Phase: N/A
Study type: Interventional

The complement C1q tumor necrosis factor-associated protein-9 (CTRP-9), which is responsible for regulating cardiovascular and metabolic functions, increases vascular relaxation by pathway dependent on AMPK / endothelial nitric oxide synthesis (eNOS). The aim of this study was to investigate CTRP-9 levels in pregnant women with preeclampsia.

NCT ID: NCT03613714 Completed - Clinical trials for Hypertension in Pregnancy

Innovation in Postpartum Care for Women With Hypertensive Disorders of Pregnancy

Start date: September 1, 2018
Phase: N/A
Study type: Interventional

Hypertensive disorders of pregnancy (HDP) affect up to 10% of mother-infant dyads and account for 7.4% of cases of maternal mortality in the United States. Prompt recognition and treatment of hypertension remain one of the key features of management of mothers affected by these conditions. Up to 41% of severe morbidity and mortality from HDP occurs after 48 hours postpartum, as postpartum blood pressures tend to peak 3-6 days after birth. For these reasons, early postpartum follow-up is recommended for women diagnosed with HDP, in the form of blood pressure (BP) evaluation by a health care provider at 7-10 days postpartum (2-5 days post-discharge from maternity care). However, barriers to follow-up limit mothers' ability to adhere to this recommendation. A potential alternative to in-office evaluation is at-home BP monitoring. At-home BP monitoring is a novel, affordable method to empower, educate, and engage postpartum women affected by HDP. Within the obstetric (OB) population, pilot studies have demonstrated the feasibility and acceptability of remote BP monitoring. Hence, the purpose of this randomized trial is to empower postpartum women affected by HDP and cared for at North Carolina Women's Hospital to perform at-home BP monitoring with the aid of digital technology.

NCT ID: NCT03576092 Completed - Clinical trials for Pregnancy Complications

Lung Ultrasound Patterns Preeclampsia

Start date: August 15, 2016
Phase:
Study type: Observational

Evaluation of lung ultrasound as a diagnostic tool in pregnant patients.

NCT ID: NCT03567551 Completed - Preeclampsia Clinical Trials

Novel Biomarkers of Preeclampsia, Aquaporin, Fatty Acid, and S110B

Start date: May 15, 2017
Phase:
Study type: Observational

This is a research study designed to help identify preeclampsia in pregnant women earlier, and possibly lead to better treatment for women preeclampsia.

NCT ID: NCT03562715 Completed - Preeclampsia Clinical Trials

microRNAs Role in Pre-eclampsia Diagnosis

Start date: November 28, 2016
Phase:
Study type: Observational

Pre-eclampsia is one of the most threatening pregnancy complications. So far neither a secure, competent therapy for PE nor effective biomarkers for a premature discovery has been achieved.The aim of our study was to identify miRNAs 136, 494 and 495 genes expression in exosomes of peripheral blood compared to umbilical cord mesenchymal stem cells conditioned media released exososomes in patients with PE, as valuable markers for PE early prediction.

NCT ID: NCT03555630 Completed - Preeclampsia Clinical Trials

Thromboelastogram in Postdelivery Preeclamptic Patients

Start date: May 22, 2018
Phase:
Study type: Observational

There are no studies evaluating the effect of aging on hemostasis of preeclamptic patients. Additionally, although there are some studies that establish normal reference values for TEG profiles in healthy term pregnant patients, conflicting results have been found in preeclampsia. Reference values are important to establish baseline parameters in cases of pre-eclampsia complicated by postpartum hemorrhage. The investigators will evaluate reference values for TEG in postdelivery preeclamptic patients and the difference between vaginal delivery and cesarean section.

NCT ID: NCT03554681 Completed - Pre-Eclampsia Clinical Trials

Prediction of Preeclampsia (PE) at 11-13 Week

Start date: December 2016
Phase:
Study type: Observational

This is an international multicentre prospective cohort study to validate the Bayes theorem based algorithms for the screening of pre-eclampsia (PE) in the first-trimester of pregnancy.