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Heart Diseases clinical trials

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NCT ID: NCT04014140 Recruiting - Clinical trials for Coronary Artery Disease

iFR Guided Coronary Artery Bypass Grafting Surgery

iCABG
Start date: April 25, 2022
Phase:
Study type: Observational

The expected outcome of better and improved patency of bypass grafts and its direct relation to pre-operative iFR measurements of stenosis as compared to direct visual physiology of stenosis in the coronary angiogram. To establish the correlation between the use of intracoronary physiology and improved graft patency at 12 months for patients undergoing CABG surgery. It is a minimum of 28 and a maximum of 100 patients single-centre proof or concept/ observational study/ pilot study.

NCT ID: NCT04004546 Recruiting - Coronary Disease Clinical Trials

Improving Medication Adherence Through a Health Literacy-based Intervention for Coronary Heart Disease Patients

Start date: March 18, 2019
Phase: N/A
Study type: Interventional

This is a multi-center pilot study to examine the effectiveness of a health literacy-based intervention to improve medication adherence and self-efficacy of medication use among individuals with coronary heart disease (CHD). The specific aims are to: i) develop a health literacy-based intervention to improve medication adherence for CHD individuals with low health literacy and ii) evaluate the effects of a health literacy-based intervention on improving medication adherence and self-efficacy in CHD individuals.

NCT ID: NCT04001283 Recruiting - Clinical trials for Coronary Artery Disease

Nitrite Effects on Cardiac Muscle in CABG

Start date: January 21, 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to test whether sodium nitrite affects the expression of cellular proteins important for metabolic and vascular function in vascular offcuts and cardiac biopsies taken from patients undergoing coronary artery bypass grafting (CABG) surgery.

NCT ID: NCT03991910 Recruiting - Clinical trials for Rheumatic Heart Disease

The Effect of Ramipril in Suppressing ST2 Expression in Rheumatic Mitral Stenosis Patients

Start date: June 27, 2019
Phase: Phase 3
Study type: Interventional

Objective propose: to investigate the effect of Ramipril in suppressing ST2 (suppression of tumorigenicity 2) in the cardiac mitral valve in patients with Rheumatic Heart Disease. We hypothesized that we hypothesized that ramipril will improve rheumatic mitral valve fibrosis through the downregulation of ST2.

NCT ID: NCT03977428 Recruiting - Clinical trials for Pulmonary Arterial Hypertension

Central China Congenital Heart Disease Associated Pulmonary Arterial Hypertension Cohort Study

CHD-PAHCS
Start date: January 1, 2019
Phase:
Study type: Observational

The study will recruit and follow up patients for five years patients newly diagnosed with congenital heart disease associated pulmonary arterial hypertension(CHD-PAH) from the investigator's hospital. The main aim of the study is to describe the aetiology, natural history and management practices of CHD-PAH in central China.

NCT ID: NCT03977129 Recruiting - Clinical trials for Primary Valvular Heart Disease With Comorbid Coronary Artery Disease

Quantitative Flow Ratio (QFR) Guided Revascularization Strategy for Patients Undergoing Primary Valve Surgery With Comorbid Coronary Artery Disease

FAVOR4-QVAS
Start date: August 4, 2019
Phase: N/A
Study type: Interventional

This is a multicenter, prospective, randomized, blinded, controlled clinical study in patients with planned primary valvular surgery and comorbid coronary artery lesions with diameter stenosis of ≥ 50%, to compare the effectiveness of an Quantitative Flow Ratio (QFR)-guided revascularization strategy and a coronary angiography (CAG)-guided revascularization strategy in preventing the incidence of composite outcome (MACE-5, including all-cause death, myocardial infarction, stroke, unplanned coronary revascularization, and new renal failure requiring dialysis) within 30 days after surgery. The study hypothesis is that the QFR-guided strategy can reduce the incidence of the MACE-5 within 30 days after surgery, as compared with the CAG-guided strategy.

NCT ID: NCT03969394 Recruiting - Heart Failure Clinical Trials

The Prognostic Role of the Right Ventricle in Patients With Heart Failure or Congenital Heart Disease

RV-STRAIN
Start date: June 1, 2017
Phase: N/A
Study type: Interventional

The objectives are 1. to validate quantification of 2D and 3D right ventricular strian measurements of right ventricular performance in cross comparison to cardiac MRI and to evaluate its relation to right ventricular fibrosis. 2. to evaluate their prognostic value in patients with heart failure with either depressed or preserved ejection fraction.

NCT ID: NCT03966729 Recruiting - Heart Failure Clinical Trials

Relationships and Differences Analysis in Heart Failure

REDEAL-HF
Start date: January 1, 2009
Phase:
Study type: Observational

This study characterizes heart failure patients who attended the University Hospital Würzburg. The primary aim is a better understanding of the relationships and differences between the subgroups HFrEF (EF < 40%), HFmrEF (EF 40-49%), and HFpEF (EF>50%), contributing to an improved diagnosis, prognosis and therapy of patients with heart failure.

NCT ID: NCT03946410 Recruiting - Vascular Diseases Clinical Trials

Danish Cardiovascular Screening Trial II

DANCAVAS-II
Start date: August 1, 2017
Phase: N/A
Study type: Interventional

This study attempts to reduce social inequality in cardiovascular health by performing an interventional screening trial on how best to decrease cardiovascular disease (CVD) among people with low social status.

NCT ID: NCT03944837 Recruiting - Clinical trials for Congenital Heart Disease

Acute Maternal Hyperoxygenation in CHD

Start date: April 26, 2019
Phase: N/A
Study type: Interventional

Congenital heart disease (CHD) is predominantly detected before birth. Using echocardiography and MRI, this study will determine whether acute exposure to maternal hyperoxygenation (MH) leads to measurable increases in fetal cerebral oxygenation from baseline in fetuses with CHD. The study aims to determine whether MH could be used as a chronic in-utero treatment strategy to promote brain growth/maturation to birth and to improve postnatal neurodevelopmental outcomes, and identify the types of CHD most likely to benefit from chronic MH.