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Myocardial Ischemia clinical trials

View clinical trials related to Myocardial Ischemia.

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NCT ID: NCT00133692 Completed - Hypertension Clinical Trials

INVEST: INternational VErapamil SR Trandolapril STudy

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

Because blood pressure affects the heart, blood vessels, kidneys, and the entire body, it is important to keep it as normal as possible. There are several different ways to control blood pressure and to prevent or limit the development of heart disease due to high blood pressure. The purpose of this study is to compare two treatments to see how well they work and the difference in their side effects. One treatment includes the use of a calcium antagonist drug (Isoptin sustained release [SR] or Verapamil SR). The other treatment excludes the calcium antagonist and may include a non-calcium antagonist drug called a beta blocker (Tenormin or Atenolol). Both treatments may also include medication called angiotensin converting enzyme (ACE) inhibitors and water pills. None of the drugs in this study are experimental, they are all approved by the Food and Drug Administration (FDA).

NCT ID: NCT00133328 Active, not recruiting - Hypertension Clinical Trials

A Morbidity-Mortality and Remodeling Study With Valsartan

Start date: January 2002
Phase: Phase 4
Study type: Interventional

The JIKEI HEART Study has been designed to investigate whether concomitant treatment with valsartan, an angiotensin II receptor blocker (ARB), in addition to conventional treatment, will improve the prognosis of 3000 Japanese patients with cardiovascular diseases.

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: NCT00130871 Completed - Clinical trials for Coronary Heart Disease

Levosimendan Pretreatment for Weaning Patients From Cardio-Pulmonary Bypass

Start date: January 2004
Phase: Phase 2
Study type: Interventional

The study evaluates the efficacy of intravenous levosimendan treatment started during a coronary artery bypass operation to wean patients from a heart lung machine.

NCT ID: NCT00130546 Completed - Clinical trials for Coronary Artery Disease

Intra-Individual Comparison of Sirolimus and Paclitaxel Coated Stent (FRE-RACE Study)

Start date: November 2004
Phase: Phase 3
Study type: Interventional

The main objective of this study is to assess the safety and effectiveness of the Sirolimus eluting Cypher Select(TM) stent in reducing angiographic in-stent late loss in de novo native coronary lesions as compared to the TAXUS(TM) Paclitaxel-eluting stent in patients presenting with two or more coronary artery stenoses (prospective, randomized, intra-individual comparison).

NCT ID: NCT00129038 Completed - Clinical trials for Coronary Arteriosclerosis

Modified-release Dipyridamole/Aspirin (200mg/25mg bd) Versus Aspirin (75mg) in Aspirin-resistant Patients

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

The primary objective of this study is to assess whether adding modified-release dipyridamole to aspirin (Asasantin Retard) has measurable effects on markers of platelet function (for example, platelet aggregation) in patients with cardiovascular disease who are known to be resistant to aspirin alone

NCT ID: NCT00127751 Completed - Stroke Clinical Trials

Heart Disease on the Mend

Start date: May 2000
Phase: Phase 2
Study type: Interventional

The primary objective of this study was to evaluate the effectiveness of a multifactor cardiovascular disease (CVD) risk reduction program using team case management in high risk patients who have low family incomes and limited access to medical care. Patients were randomized to case management (99) or usual care (49) with baseline, 6-month and 12-month evaluations of CVD risk factors, clinical status and quality of life.

NCT ID: NCT00124371 Completed - Clinical trials for Coronary Artery Disease

Programme to Optimise Risk Factors in Patients Waiting for Coronary Artery Bypass Surgery

Start date: January 2003
Phase: Phase 2/Phase 3
Study type: Interventional

The time spent waiting for heart surgery can be extremely stressful. This programme aims to address this by providing a home-based, nurse-led support and education programme. Patients will be followed up in their own homes monthly by a cardiac nurse and given lifestyle advice and information to prepare them for surgery. This will be evaluated to test whether providing this support improves patients’ anxiety and quality of life while they wait and also whether their blood pressure, weight and cholesterol are reduced and they have a smoother recovery as a consequence.

NCT ID: NCT00124332 Completed - Clinical trials for Coronary Atherosclerosis

STRADIVARIUS (Strategy To Reduce Atherosclerosis Development InVolving Administration of Rimonabant - the Intravascular Ultrasound Study)

Start date: January 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if rimonabant 20 mg once daily (od) administered during 18-20 months will reduce progression of coronary atherosclerosis as assessed by intravascular ultrasound (IVUS) when administered on top of standard behavioral and pharmacological therapy given as needed, in patients with abdominal obesity associated with current smoking and/or metabolic syndrome.

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.