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Heart Disease clinical trials

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NCT ID: NCT03097120 Completed - Heart Disease Clinical Trials

The Estrogen Replacement and Atherosclerosis Trial ; Primary Outcome Measure is Mean Minimal Coronary Artery Diameter After Avg of 3.2 Yrs.

ERA
Start date: January 1995
Phase: Phase 3
Study type: Interventional

Background: Heart disease is a major cause of illness and death in women. To understand better the role of estrogen in the treatment and prevention of heart disease, more information is needed about its effects on coronary atherosclerosis and the extent to which concomitant progestin therapy may modify these effects. Methods: The investigators randomly assigned a total of 309 women with angiographically verified coronary disease to receive 0.625 mg of conjugated estrogen per day, 0.625 mg of conjugated estrogen plus 2.5 mg of medroxyprogesterone acetate per day, or placebo. The women were followed for a mean (±SD) of 3.2±0.6 years. Base-line and follow-up coronary angiograms were were analyzed by quantitative methods. Follow-up coronary angiograms were obtained after an average of 3.2 years of follow up.

NCT ID: NCT03059472 Completed - Obesity Clinical Trials

Strong Hearts for New York: A Rural Heart Disease Prevention Study

Start date: March 31, 2017
Phase: N/A
Study type: Interventional

Strong Hearts for New York 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. Our aim is to better understand how changes in lifestyle can affect the health of rural women and others in their communities.

NCT ID: NCT02955238 Completed - Clinical trials for Type 2 Diabetes Mellitus

Latinos Understanding the Need for Adherence

LUNA
Start date: August 2009
Phase: N/A
Study type: Interventional

The Latino population in the United States is increasing in size; is diverse in culture, backgrounds and countries of origin; is experiencing unique influences from social and behavioral acculturation to the U.S.; is reported nationally to have lower rates of heart disease; is reported to have increased prevalence of diabetes and asthma; and is generally poorer and less educated (NHLBI working Group, 2003). They represent an important target population for disparities research. In particular Latinos accessing care in Community Health Centers in the United States represent an ideal population for conducting disparities research because lack of access to care is minimized through various governmental health insurance support mechanisms. This study will build on existing relationships to conduct the proposed study, using expertise in epidemiologic, behavioral and genetic research in an effort to promote a coordinated, comprehensive, interdisciplinary and focused research effort to improve the care being delivered to indigent Latinos at-risk for and with CVD.

NCT ID: NCT02935491 Completed - Heart Disease Clinical Trials

4 Cities for Assessing CAlcification PRognostic Impact After TAVI

C4CAPRI
Start date: April 2016
Phase: N/A
Study type: Observational

Transcatheter Aortic Valve Implantation (TAVI) indications are progressing rapidly as an alternative to conventional surgery for aortic stenosis cure. Despite a high rate of procedural success, some patients do not benefit from the procedure. The investigators hypothesis is that aortic stiffness may be of major prognostic significance after stenosis relief. The aim of this study is to test the prognostic impact of aortic stiffness estimated by the volume of calcifications of the thoracic aorta on the CT-scan performed systematically before the procedure. This prognostic value will be assessed in 4 independent cohorts issued from 4 french cities (Lyon, Rouen, Paris, Clermont-Ferrand).

NCT ID: NCT02923518 Completed - Heart Disease Clinical Trials

Cardiac Screening of Middle Aged and Older Women and Men (Master Athletes)

MASTERSCREEN
Start date: October 2016
Phase:
Study type: Observational

In 2010 there was published new European recommendations for assessment of adult and elderly men and women, who want to start with physical activity and/or participate in endurance contests. In this study we want to test if a group of people with positive score on a self-reported questionnaire and/or high-risk score in a risk scoring system (NORRISK) have more undetected heart diseases than a control group with no reported or detected risk factors.

NCT ID: NCT02894632 Completed - Heart Disease Clinical Trials

MR Compatible Accelerometer for Respiratory MOTion Measurement

MARMOT
Start date: July 2013
Phase: N/A
Study type: Interventional

A novel magnetic resonance (MR) compatible accelerometer for respiratory motion sensing (MARMOT) has been developed as a surrogate of the vendors' pneumatic belts. The aim is to model and correct respiratory motion for free-breathing thoracic-abdominal MR imaging and to simplify patient installation.

NCT ID: NCT02887820 Completed - Heart Disease Clinical Trials

Evaluating the Use of Thromboelastography (TEG) in Patient's Requiring Extracorporeal Membrane Oxygenation (ECMO)

Start date: December 15, 2017
Phase: N/A
Study type: Interventional

This is a pilot study that seeks to evaluate the feasibility and safety of using a TEG algorithm in addition to traditional laboratory tests to guide transfusion and coagulation management of ECMO patients.

NCT ID: NCT02836431 Completed - Heart Disease Clinical Trials

Pharmacokinetic Study of Dexmedetomidine After Intra-nasal Dosing in Children

Start date: January 2016
Phase: Phase 1
Study type: Interventional

This research study is examining the absorption of the sedative dexmedetomidine (DEX) in the blood when given by nasal spray. The study will help us determine the best dosing amount for children undergoing sedation or anesthesia with DEX.

NCT ID: NCT02813668 Completed - Obesity Clinical Trials

Worksite Lifestyle Program for Reducing Diabetes and Cardiovascular Risk in India

Start date: May 2, 2017
Phase: N/A
Study type: Interventional

This study will test the implementation, effectiveness, cost-effectiveness, and acceptability of a worksite lifestyle improvement program that includes lifestyle education classes led by trained individuals from the worksite and improvements in the worksite environment that will make it easier for employees at risk for diabetes or with unmedicated diabetes to lose weight, exercise more, and eat a healthier diet. A total of 2000 participants across 10 worksites in South, Central, and East India will be involved in this study.

NCT ID: NCT02775565 Completed - Heart Disease Clinical Trials

Initial Experience With the AngioVac Venous Drainage Cannula

Start date: February 2016
Phase: N/A
Study type: Observational

This is a retrospective, record-based study of approximately 100 patients across up to 12 centers within the United States. All patients who have been treated with the AngioVac Venous Drainage Cannula and the Extracorporeal Circuit will be considered for study participation. Eligible subject must meet all of the inclusion criteria and none of the exclusion criteria to be considered enrolled in the study. The purpose of the study is to describe initial experience with the AngioVac Venous Drainage Cannula and the Extracorporeal Circuit.