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Peripartum Cardiomyopathy clinical trials

View clinical trials related to Peripartum Cardiomyopathy.

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NCT ID: NCT04144660 Completed - Cardiogenic Shock Clinical Trials

"Treatment Use of ECMO In Pregnancy or Peripartum Patient."

Start date: October 28, 2019
Phase:
Study type: Observational

The goal of this study is to describe the use of ECMO (Extracorporeal Membrane Oxygenation) in the pregnant or peripartum patient.

NCT ID: NCT04049136 Completed - Obesity Clinical Trials

NT-proBNP Levels and Obesity in Pregnancy

Start date: July 15, 2019
Phase:
Study type: Observational

A screening modality to help categorize obese pregnant women as high or low probability for heart failure would be helpful in the evaluation of the obese pregnant women with dyspnea. Outside of pregnancy, measurement of brain natriuretic peptide (BNP) or amino-terminal pro-brain natriuretic peptide (NT-proBNP) is recommended in the evaluation of acute dyspnea and in the diagnosis of heart failure. During pregnancy, elevated BNP has been associated with adverse cardiovascular events, while normal BNP levels have been observed in healthy pregnancies. While BNP levels outside of pregnancy have been shown to be lower in obese patients variations in BNP levels by body mass index (BMI) in pregnancy have not been studied. Before BNP can be deemed a reliable screening test for heart failure in obese pregnant women, normal BNP values in the setting of obesity and pregnancy need to be established. We therefore propose the following specific aims: Objective 1: Compare mean plasma NT-proBNP levels in the third trimester, immediately postpartum, and at 4-6 weeks postpartum between obese pregnant women without cardiovascular disease and non-obese pregnant women without cardiovascular disease. We hypothesize that mean plasma NT-proBNP levels in obese pregnant women without pre-existing cardiovascular disease will be significantly lower than levels in non-obese pregnant women. Objective 2: Assess whether plasma NT-proBNP levels in pregnancy correlate with BMI. We hypothesize that there will be an inverse correlation between plasma NT-proBNP levels and BMI in our pregnant cohort similar to that seen outside of pregnancy.

NCT ID: NCT03907267 Completed - Clinical trials for Peripartum Cardiomyopathy

Taurine in Peripartum Cardiomyopathy

Start date: January 1, 2015
Phase: Phase 2/Phase 3
Study type: Interventional

Taurine as an adjunct for early left ventricular recovery in peripartum cardiomyopathy

NCT ID: NCT03081949 Completed - Clinical trials for Peripartum Cardiomyopathy

Peripartum Cardiomyopathy in Nigeria Registry

PEACE
Start date: June 12, 2017
Phase: Phase 4
Study type: Interventional

Peripartum cardiomyopathy (PPCM) is a global disease with significant morbidity and mortality, and Nigeria probably has the highest burden of the disease in the world. Unfortunately, much about the disease including its aetiology, epidemiology and treatment is not yet well described. This will be a prospective, national, multicenter cohort study, conducted in centres in Nigeria. It is expected that approximately 500 patients with PPCM and 500 apparently healthy pregnant women will be recruited over a 6-month period with follow-up at 3-monthly intervals for 18 months.

NCT ID: NCT00998556 Completed - Clinical trials for Peripartum Cardiomyopathy

Effect of Bromocriptine on Left Ventricular Function in Women With Peripartum Cardiomyopathy

PPCM
Start date: June 2010
Phase: Phase 2
Study type: Interventional

This is a randomized, controlled clinical trial to evaluate the efficacy and safety of bromocriptine for improvement of left ventricular function of women with Peripartum cardiomyopathy (PPCM). A Multi center trial in Germany.