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Heart Disease clinical trials

View clinical trials related to Heart Disease.

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NCT ID: NCT02767154 Completed - Heart Disease Clinical Trials

Dextran-based Priming vs. Crystalloid and Mannitol-based Priming Solution in Adult Cardiac Surgery

Start date: May 2016
Phase: Phase 2
Study type: Interventional

This study will compare two priming solutions for extracorporeal circulation, one based on Dextran 40, one based on crystalloid and mannitol. Primary endpoint is oncotic pressure during cardiopulmonary bypass. Secondary endpoints included fluid balance and organ functions.

NCT ID: NCT02736344 Completed - Heart Disease Clinical Trials

BIONICS - Pharmacokinetics (PK) Trial

BIONICS
Start date: April 2016
Phase:
Study type: Observational

The BioNIR Ridaforolimus Eluting Coronary Stent System is a single use device/drug combination product comprising: - Stent - mounted Cobalt Chromium (CoCr) alloy based stent - Delivery System - Rapid Exchange (RX) Coronary System - Polymer matrix coating - Poly n-butyl methacrylate (PBMA) and polymer coating (CarboSil®) - Ridaforolimus drug - Chemical Abstracts Service (CAS) Registry Number: 572924-54-0 The product is indicated for improving coronary luminal diameter in patients with symptomatic heart disease due to lesions in vessels with reference diameters of 2.5mm to 4.25mm, including complex lesions.

NCT ID: NCT02687763 Completed - HEART DISEASE Clinical Trials

Safety and Efficacy of ProQuad® in Children 6-24 Month Being Evaluated for Solid Organ Transplant

ProQuad®
Start date: December 2015
Phase: Early Phase 1
Study type: Interventional

A prospective, multisite study to evaluate the Impact of Measles, Mumps, Rubella and Varicella ProQuad® vaccination in pediatric patients 6-24 months of age who are being considered and/or evaluated for any solid organ transplant (heart, liver or kidney)

NCT ID: NCT02684331 Completed - Clinical trials for Diabetes Mellitus, Type 2

CMR in Type 2 Diabetes Mellitus Patients

Start date: January 2016
Phase:
Study type: Observational

The study will be performed as a cross-sectional survey. 300 Type 2 diabetes patients (T2DM), with or without known cardiovascular disease, will be recruited from the diabetes outpatient clinic, Slagelse Hospital. The patients will undergo echocardiography, Cardiac magnetic resonance imaging (CMR), clinical examination and will be asked to fill out questionnaires. This study project sets out to answer the following hypotheses: 1. Patients with T2DM have an increased risk of developing diastolic dysfunction. Using CMR, the investigators wish to measure left ventricle peak filling rate and passive atrial emptying fraction as a measure of cardiac diastolic function. The investigators hypothesize that classic T2DM markers such as levels of urinary albumin excretion, retinopathy, autonomic neuropathy, hypertension, dyslipidemia, elevated HgbA1c, T2DM duration, etc. are associated with pathological findings by CMR. 2. Patients with T2DM have impaired left ventricle myocardial perfusion as determined by gadolinium contrast CMR. The investigators hypothesize that the classic markers and risk factors mentioned above, are associated with left ventricle myocardial hypoperfusion as determined by gadolinium contrast CMR.

NCT ID: NCT02523144 Completed - Heart Disease Clinical Trials

Dexmedetomidine in Children Having Transthoracic Echocardiography

Start date: September 2014
Phase: Phase 4
Study type: Interventional

Sedation Techniques for children undergoing transthoracic echocardiography (TTE).

NCT ID: NCT02504762 Completed - Diabetes Clinical Trials

HYbrid CoronAry Revascularization in DiabeticS

HYCARDS
Start date: August 2015
Phase: N/A
Study type: Interventional

To evaluate whether an HCR strategy is more or less effective than conventional coronary artery bypass grafting (cCABG), in diabetic patients with multivessel CAD involving the left anterior descending artery (LAD), who do not present in the context of acute ST-elevation myocardial infarction (STEMI).

NCT ID: NCT02499731 Completed - Obesity Clinical Trials

Strong Hearts: Rural CVD Prevention

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

Strong Hearts, Healthy Communities is a research study which aims to reduce cardiovascular disease (CVD), improve quality of life, and reduce CVD related health care costs in rural communities. The investigators' aim is to better understand how changes in lifestyle can affect the health of rural women and others in their communities.

NCT ID: NCT02376244 Completed - Heart Disease Clinical Trials

The Health Impact of High Intensity Exercise Training With Intervals During Cardiac Rehabilitation

Start date: September 2015
Phase: N/A
Study type: Interventional

Cardiac rehabilitation is a program designed to help patients regain good health through lifestyle change after a heart attack, heart surgery or other heart problems. Patients will take part in exercise sessions and education lessons, tailored to meet their personal needs. The exercise training component of cardiac rehabilitation may be delivered as intervals of short intense sessions (also known as high intensity intervals) or the current standard care of longer but less intense sessions (moderate intense intervals). Both exercises have been shown to increase fitness levels and also prevent future risk of heart disease. The purpose of this study is to determine the efficacy and safety of high intensity interval exercise training (HIIT) in patients who had a recent cardiac revascularization procedure or recovering from a heart attack, in comparison to current standard of moderate intensity exercise training in terms of their physical fitness and psychological well-being.

NCT ID: NCT02344433 Completed - Stroke Clinical Trials

Using Virtual Counselors to Overcome Genetic Literacy Barriers

VICKY
Start date: November 2016
Phase: N/A
Study type: Interventional

A Relational Agent (RA) "virtual counselor" (VICKY: VIrtual Counselor for Knowing Your Family History) has been developed to collect family health history information for common health conditions including heart disease, stroke, diabetes, hypertension and various cancers. In this study, the investigators will conduct a randomized controlled trial (RCT) to compare the efficacy of using VICKY to the existing My Family Health Portrait (MFHP) tool for collecting family health history information among an underserved primary care patient population. The primary aims of the study are to 1) evaluate the efficacy of VICKY versus MFHP for collecting accurate family health histories and 2) determine whether accuracy varies as a function of health literacy. This project will obtain validation data on the efficacy of both VICKY and MFHP for collecting accurate family history data among an underserved patient population, in two languages (English and Spanish). The study will determine whether a virtual counselor can overcome many of the existing barriers to using traditional web-based family history tools.

NCT ID: NCT02302612 Completed - Hypertension Clinical Trials

The CREATE Wellness Study

Start date: January 2015
Phase: N/A
Study type: Interventional

Cardiovascular disease (CVD) is the leading cause of death in the U.S. Efforts to improve CVD risk factors often fall short in complex patients with multiple co-morbid conditions, a growing, expensive, and high-risk segment of the U.S. population. The investigators are testing a multi-component behavioral intervention designed to help complex patients with CVD and other concurrent chronic conditions to become more effective agents of their own care.