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Pregnancy Complications clinical trials

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NCT ID: NCT05720650 Withdrawn - Preeclampsia Clinical Trials

B Vitamin Deficiency and Pregnancy Complications

Start date: June 1, 2023
Phase:
Study type: Observational

This case-control study aims to investigate the association between B vitamins and gestational hypertension or preeclampsia.

NCT ID: NCT04274803 Withdrawn - Clinical trials for Antiphospholipid Syndrome in Pregnancy

Dose Intralipid Infusion Reduces Pregnancy Complications Caused by Antiphospholipid Antibody Syndrome?

Start date: April 1, 2020
Phase: Phase 4
Study type: Interventional

This study will address the value of adding intralipid infusion in reducing pregnancy complications related to antiphospholipid syndrome

NCT ID: NCT03395652 Withdrawn - Clinical trials for Pregnancy Complications

Maternal Physical Activity and Pregnancy Outcome

Start date: January 2018
Phase:
Study type: Observational

The aim of this study is to investigate the impact of maternal physical activity during pregnancy on pregnancy outcome. Primary, fetal growth during pregnancy abd birth weight will be examined.

NCT ID: NCT03245970 Withdrawn - Preeclampsia Clinical Trials

Impedance Cardiography to Decrease the Risk of Preeclampsia

Start date: April 24, 2017
Phase: Early Phase 1
Study type: Interventional

To determine if the use of impedance cardiography can identify appropriate medications for use in treating chronic hypertensive patients to decrease the risk of preeclampsia.

NCT ID: NCT01965054 Withdrawn - Clinical trials for Intrahepatic Cholestasis of Pregnancy

The Use of Fish Oil Supplementation in Treatment of Intrahepatic Cholestasis of Pregnancy

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

Intrahepatic cholestasis of pregnancy (ICP) is a unique disease of the liver resulting in abnormal bile acid levels and liver function. The incidence of ICP ranges from 0.1 - 15.6%. Women diagnosed with ICP most often present with itching, which may be severe. More concerning, however, is the impact of ICP on adverse fetal and pregnancy outcomes, including preterm delivery, meconium exposure, fetal demise, and increased neonatal respiratory complications. The risk for fetal demise has been estimated to be 1-3%. The mechanism of fetal demise in ICP is unknown, and therefore cannot be reliably predicted. There is evidence to suggest that extremely elevated bile acids levels are associated with worse fetal outcomes, particularly levels greater than 40 μmol/L. Ursodeoxycholic acid (UDCA) has anticholestatic effects, and is used to treat a variety of cholestatic liver diseases. Many studies have demonstrated superiority of UDCA over other agents, including dexamethasone and cholestyramine, for relief of maternal pruritus, improvement in transaminitis, reduction in serum bile acid concentrations, and improved pregnancy outcomes. As a result, UDCA is now widely used as first-line treatment for symptomatic relief in patients with ICP. Docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA) are two omega-3 long chain polyunsaturated fatty acids found in fish. DHA is known to play a key role in early fetal brain development, and has been associated with modest beneficial effects on neurodevelopmental and cognitive outcomes in children. In neonates with parental nutrition-induced cholestasis (PN-cholestasis), parental fish oil has been shown to be hepatoprotective not only for treatment of PN-cholestasis, but for prevention of cholestasis in premature infants at risk for the disease. Our hypothesis is that fish oil supplementation with DHA in women with ICP who are treated with UDCA will increase the rate of decline in serum total bile acid levels. The incidence of ICP at a single hospital center in Queens, NY is estimated to be 5% secondary to a high concentration of patients from high-risk ethnic groups. High risk patients with bile acid levels greater than or equal to 40 μmol/L are managed aggressively with inpatient admission for continuous fetal monitoring, treatment with UDCA, and serial total bile acid levels weekly. These are patients are routinely offered early delivery after documented fetal lung maturity between 36 and 37 weeks gestation, or for any signs of fetal distress. This study is a prospective randomized controlled trial comparing weekly serum total bile acid levels in women admitted for inpatient management of ICP among women supplemented with a standard prenatal vitamin versus supplementation with a prenatal vitamin and DHA.