Clinical Trials Logo

Ischemic Heart Disease clinical trials

View clinical trials related to Ischemic Heart Disease.

Filter by:

NCT ID: NCT00175240 Completed - Coronary Disease Clinical Trials

Enhancing the Secondary Prevention of Coronary Artery Disease

Start date: March 2005
Phase: Phase 4
Study type: Interventional

People with coronary artery disease can reduce their chance of having a heart attack by making healthy lifestyle choices (diet, exercise, quitting smoking,etc.). There are also many medications that have been proven to reduce the risk of heart attacks and may even help people live longer. This study will look at different ways of improving the use of these beneficial medications to enhance the quality of care for people with this condition.

NCT ID: NCT00150826 Completed - Clinical trials for Ischemic Heart Disease

QWISE - Study of Quinapril in Women With Chest Pain, Coronary Flow Reserve Limitations and Evidence of Myocardial Ischemia

Start date: May 2000
Phase: Phase 4
Study type: Interventional

INDICATION Microvascular angina. OBJECTIVES To investigate the effect of ACE (angiotensin converting enzyme) inhibition (quinapril) in improving coronary microvascular function. PATIENT POPULATION Women who meet the National Heart, Lung and Blood Institute-sponsored WISE (Women Ischemia Syndrome Evaluation) study criteria of chest discomfort, coronary flow reserve limitations and evidence for myocardial ischemia in the absence of significant coronary artery stenosis. STUDY DESIGN A prospective, randomized, placebo-controlled, comparative trial. TREATMENT Quinapril 80 mg/d versus placebo for four months. PRIMARY EFFICACY PARAMETER(S) Coronary flow reserve (CFR) at Week 16 adjusted for baseline CFR, treatment group assignment, site-specific variables, and site by treatment effects. SECONDARY EFFICACY PARAMETERS Week 16 change in chest discomfort as measured by the Seattle Angina Questionnaire adjusting for baseline values, site, and site by treatment effects. SAFETY PARAMETERS Hematology, blood chemistries, blood pressure and pulse, and frequency and occurrence of adverse events. STATISTICAL RATIONALE AND ANALYSIS A statistical rationale for the number of patients in the study has been provided. Interim analyses are planned after 15 patients have been enrolled in each group. ANTICIPATED TOTAL NUMBER OF PATIENTS 78 (39 per group). ANTICIPATED NUMBER OF PATIENTS AT EACH SITE Approximately 26

NCT ID: NCT00149227 Completed - Stroke Clinical Trials

Add-on Effects of Valsartan on Morbi- Mortality (KYOTO HEART Study)

Start date: January 2004
Phase: Phase 4
Study type: Interventional

The KYOTO HEART Study is to assess the add-on effect of valsartan, an Angiotensin-Receptor Blocker, on top of the conventional treatment in high risk patients in Japan with hypertension in terms of the morbidity and mortality.

NCT ID: NCT00139802 Completed - Clinical trials for Ischemic Heart Disease

DANish Multicenter STENT Trial

Start date: April 1997
Phase: Phase 4
Study type: Interventional

The purpose of the study was to evaluate procedural and late outcome of coronary artery stenting using 2 different unmounted stents

NCT ID: NCT00135850 Completed - Clinical trials for Ischemic Heart Disease

The Effect of Mobilized Stem Cell by G-CSF and VEGF Gene Therapy in Patients With Stable Severe Angina Pectoris

Start date: March 2003
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this study was to evaluate the mobilization of non-haematopoietic mesenchymal and haematopoietic stem cells from the bone marrow with granulocyte colony stimulating factor (G-CSF) treatment alone and in combination with vascular endothelial growth factor (VEGF) gene therapy in patients with severe chronic occlusive coronary artery disease.

NCT ID: NCT00131040 Completed - Clinical trials for Ischemic Heart Disease

Investigation of Leukocyte Trafficking Into Skin Blisters During Cardiopulmonary Bypass

Start date: January 2003
Phase: N/A
Study type: Interventional

The purpose of this study was to see if the heart-lung machine involved in cardiac surgery increases the movement of activated white blood cells from the bloodstream into the patient's tissues and also to see if aprotinin usage during surgery reduces this effect.

NCT ID: NCT00123981 Completed - Clinical trials for Ischemic Heart Disease

The Danish On-pump, Off-pump Randomization Study (DOORS)

Start date: January 2005
Phase: N/A
Study type: Interventional

Background: Coronary artery bypass grafting (CABG) can be performed either with or without the use of cardiopulmonary bypass (CPB) to obtain myocardial re-vascularisation. The investigators hypothesize that CABG without the use of CPB may reduce the risk of perioperative death, stroke, myocardial infarction and other serious complications. The aim of the present study is to compare the incidence of complications and the clinical efficacy of CABG with and without the use of CPB in elderly patients.

NCT ID: NCT00041938 Completed - Stroke Clinical Trials

Warfarin Versus Aspirin in Reduced Cardiac Ejection Fraction (WARCEF) Trial

WARCEF
Start date: October 2002
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine which of two treatments, Warfarin or aspirin, is better for preventing death and stroke in patients with poor heart function. We are now transitioning into the sub-analysis part of the WARCEF patient data. The study has recently completed data analysis for its Primary Aim. All randomized patients have completed their follow up. All study related procedure as per the protocol has been completed. We are now in the extension phase of the study to obtain more patient data to address further aims of the study. No new procedures are performed and data already in place at the sites will be collected (EKG and echocardiograms). The aims for this study extension are: - To assess progression of cardiac dysfunction over time among heart failure patients - To correlate prognosis with cardiac dysfunction

NCT ID: NCT00032630 Completed - Clinical trials for Ischemic Heart Disease

Outcomes Following Myocardial Revascularization: On and Off Cardiopulmonary Bypass

ROOBY
Start date: April 2002
Phase: Phase 3
Study type: Interventional

Ischemic heart disease is one of the most frequent diagnoses in the VA system. Moreover, 5,819 coronary artery bypass graft (CABG-only) procedures were performed in the VA in Fiscal Year (FY) 1999. Throughout VA and non-VA cardiac surgery programs nationwide, myocardial revascularization is now being performed using two surgical techniques. One technique is performed with cardiopulmonary bypass (CPB) usually with cardioplegic arrest ("on-pump") and the other without CPB on a beating heart ("off-pump"). The overall purpose of this proposed randomized, controlled, clinical trial is to rigorously evaluate the impact of using an on-pump versus off-pump surgical technique for coronary artery bypass graft (CABG-only) procedures (performed with a traditional median sternotomy incision) upon patient clinical outcomes and resource utilization.

NCT ID: NCT00013104 Completed - Clinical trials for Ischemic Heart Disease

Implementation of Ischemic Heart Disease Clinical Practice Guidelines

Start date: n/a
Phase: N/A
Study type: Observational

The purpose of this study is to design and evaluate targeted implementation strategies to fully integrate the VHA clinical practice guidelines for ischemic heart disease into VHA clinical practice. Effectively implementing the guideline will enhance the quality, appropriateness, timeliness, and cost effectiveness of care delivered to veterans with ischemic heart disease.