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Myocardial Ischemia clinical trials

View clinical trials related to Myocardial Ischemia.

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NCT ID: NCT00596661 Completed - Clinical trials for Coronary Artery Disease

The TRIMAXX Coronary Stent Trial

Start date: May 2004
Phase: Phase 1
Study type: Interventional

The primary objective of the trial is to demonstrate the safety and feasibility of treating coronary artery lesions which have not been previously treated with the TRIMAXX Coronary stent system as compared to the reported results for commercially available non-drug eluting coronary stent systems which are indicated for the same treatments.

NCT ID: NCT00596479 Completed - Clinical trials for Coronary Artery Disease

Filgrastim for the Promotion of Collateral Growth in Patients With CAD

Start date: November 2004
Phase: N/A
Study type: Interventional

The purpose of this study in humans with stable coronary artery disease (CAD) treatable by PCI (percutaneous coronary intervention) is to evaluate the safety and efficacy of subcutaneous delivery of recombinant granulocyte colony stimulating factor rG-CSF (Filgrastim, Neupogen®, Amgen Switzerland) with regard to the promotion of collateral growth.

NCT ID: NCT00595673 Completed - Clinical trials for Coronary Artery Disease

Safety and Efficacy Study of PB127 Ultrasound Contrast Agent in Patients With Suspected Coronary Artery Disease 007

Start date: July 2002
Phase: Phase 3
Study type: Interventional

This trial is to compare PB127 echocardiography to other heart imaging studies.

NCT ID: NCT00595647 Terminated - Clinical trials for Coronary Artery Disease

Study to Test the Efficacy and Safety of Drug Eluting vs. Bare-Metal Stents for Saphenous Vein Graft Interventions

BASKET-SAVAGE
Start date: February 2008
Phase: Phase 4
Study type: Interventional

Prospective multicenter controlled randomized trial to compare the safety and efficacy of drug eluting vs. bare metal stents in percutaneous coronary interventions of saphenous vein grafts. Hypothesis: Survival and outcome will be significantly better in patients receiving DES than in patients receiving BMS regarding both short-term and long-term outcome.

NCT ID: NCT00595244 Completed - Clinical trials for Coronary Artery Disease

Safety and Efficacy Study of PB127 Ultrasound Contrast Agent in Patients With Suspected Coronary Artery Disease

Start date: July 2002
Phase: Phase 3
Study type: Interventional

This trial is to compare PB127 echocardiography to other heart imaging studies.

NCT ID: NCT00594698 Completed - Clinical trials for Coronary Artery Disease

Familiarization and Safety Study of PB127 Ultrasound Contrast Agent

Start date: February 2002
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to evaluate preparation and administration of PB127, echocardiographic images obtained during PB127 administration, and evaluate the safety of PB127.

NCT ID: NCT00591760 Completed - Heart Failure Clinical Trials

Growth Hormone Deficiency in Chronic Heart Failure: A Preliminary Trial

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

The aim of this study is to investigate the potential benefits of the correction of growth hormone (GH) deficiency with GH replacement therapy in patients with chronic heart failure due to left ventricular systolic dysfunction.

NCT ID: NCT00590629 Completed - Clinical trials for Coronary Artery Disease

Benefit of Elevation of HDL-C on Cardiovascular Outcomes in Women

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

Several risk factors including high cholesterol contribute to heart disease. We know that lowering triglycerides and raising HDL (protective cholesterol) in men reduces the risk for heart disease. We expect that women will share this same benefit because the combination of high triglycerides and low HDL appears to be a more important risk for heart disease in women. Niacin reduces triglycerides and raises HDL. We also expect to see improvement in markers of inflammation and clot formation and blood vessel health, which we hypothesize should all confer a reduced risk of heart disease in women. Women already taking lipid lowering statin will receive niacin therapy. We will measure blood lipid levels, markers of inflammation and clotting as well as a non-invasive measure of blood vessel reactivity. After 3 months of therapy we will repeat these measures.

NCT ID: NCT00590291 Terminated - Clinical trials for Coronary Artery Disease

Molecular Determinants of Coronaruy Artery Disease

GeneQuest
Start date: January 1995
Phase:
Study type: Observational

The purpose of this study is to discover genes that may cause Coronary Artery Disease (CAD) or Arteriovenous Malformation (AVM).

NCT ID: NCT00590200 Active, not recruiting - Clinical trials for Cardiovascular Diseases

GeneBank at the Cleveland Clinic: Molecular Determinants of Coronary Artery Disease

GATC
Start date: January 2001
Phase:
Study type: Observational

This proposal delineates a research plan to collect blood from patients undergoing heart catheterization or who have had a heart catheterization within one year and are coming in for outpatient appointments, or who have scheduled cardiac CT scans at the Cleveland Clinic over a five-year period for the purpose of establishing a gene bank registry. In addition, the University of North Carolina at Chapel Hill will enroll 1,000 non-Caucasian patients and MetroHealth Medical center in Cleveland will enroll 1,000 non-Caucasian patients. The blood collected will be processed to create a repository of DNA, lymphoblastoid cell line immortalization on selected patient populations, plasma and serum. The DNA will be amplified in certain patient populations to preserve the quantity. Along with a sample of blood collected from individual patients, a concise general medical history, demographic data, electrocardiographic data, echocardiographic data (available for about 55% of patients at the present time), and laboratory data will be collected. A short interview will take place after enrollment during the outpatient visit or hospital stay, or may be conducted via phone call after enrollment. All the clinical data gathered will be compiled in GATC heart center database, and would be stored in a format where a culmination of clinical findings, i.e. representing a disease of interest, can be used to search the database to identify the blood samples of all patients with such characteristics for further study.