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Ischemia clinical trials

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NCT ID: NCT00760708 Terminated - Coronary Disease Clinical Trials

Circulating Adenosine Levels Before and After Intravenous (IV) Persantine

Start date: September 2005
Phase:
Study type: Observational

Persantine is a drug that is routinely used to determine blood flow to the heart in the diagnosis of coronary heart disease. Persantine causes an increase in the adenosine level in the blood. Adenosine is a naturally occurring substance in the body that can increase blood flow. Adenosine is normally removed from the bloodstream by an adenosine transporter, which is a protein that takes up adenosine from the blood into cells. The increase in adenosine levels in the blood is variable, and the cause for this variability is unknown. A mutation for this transporter gene may contribute to this variability, and may alter its function. Thus, the purpose of this study is to determine the relationship between the mutation and the transporter function.

NCT ID: NCT00760357 Completed - Clinical trials for Critical Limb Ischemia

A Retrospective Analysis of Patients With Full Thickness Wounds in Limbs With Critical Ischemia

Start date: April 2007
Phase: N/A
Study type: Observational

Once the patients are identified that have a full thickness wound on a limb clearly identified as having critical limb ischemia, these patients will be evaluated. The data that will be extracted from each chart will include patient's age, patient's gender, number of office visits, presence of diabetes, presence of osteomyelitis, type and amount of antibiotic administered, number of hyperbaric oxygen treatments, and if the wound healed.

NCT ID: NCT00756249 Completed - Clinical trials for Acute Ischemic Stroke

Safety Study of Carbamylated Erythropoietin (CEPO) to Treat Patients With Acute Ischemic Stroke

Start date: October 2007
Phase: Phase 1
Study type: Interventional

The primary purpose of the study is to determine whether carbamylated erythropoietin (CEPO) is a safe treatment for patients who have suffered an acute ischemic stroke.

NCT ID: NCT00754429 Completed - Ischemic Stroke Clinical Trials

The Effect of Losartan Versus Amlodipine-based Therapy in Ischemic Stroke (0954-338)(COMPLETED)

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

To compare the effect of losartan vs amlodipine-based antihypertensive therapy on atherosclerotic inflammatory markers and cerebrovascular regulation in Ischemic stroke patients.

NCT ID: NCT00753025 Completed - Clinical trials for Lower Extremity Ischemia

Autologous Bone Marrow For Lower Extremity Ischemia Treating

Start date: October 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether autologous bone marrow derived cells and isolated CD133+ fraction are effective in the treatment limb ischemia

NCT ID: NCT00747656 Completed - Clinical trials for Myocardial Infarction

Prehospital Evaluation and Economic Analysis of Different Coronary Syndrome Treatment Strategies - PREDICT

PREDICT
Start date: February 2009
Phase: N/A
Study type: Observational

Despite remarkable gains in treatment over the last decade short-term mortality for those who survive to hospital with AT-elevation acute myocardial infarction (STEMI) remains high (5%-10%). Different studies have pointed out that reperfusion (intravenous fibrinolysis or percutaneous coronary interventions (PCI) and its timing are critical in decreasing STEMI patients' mortality. Studies of prehospital 12 lead electrocardiograms (12 lead PHECG) with advance emergency department (ED) notification suggest that there is a time to treatment advantage with this intervention. The use of 12 lead PHECG is not currently universal and part of standard treatment throughout the province. The purpose of the study is to follow STEMI study subjects during standard treatments and to compare the outcomes of subjects that received 12 lead PHECG with advanced ED notification in mixed rural/urban areas with outcomes of subjects treated in areas with only 3 lead PHECG monitoring and indirect ED notification. The investigators hypothesize that there will be a survival benefit for study subjects with 12 lead PHECG and advance ED notification in rural and urban environments through a reduction in door-to-reperfusion time and that 12 lead PHECG will be a cost-saving technology for the province of Ontario.

NCT ID: NCT00747279 Recruiting - Clinical trials for Acute Ischemic Stroke

Comparison of Two Strategies for Glycemic Control in Acute Ischemic Stroke

Start date: June 2007
Phase: Phase 4
Study type: Interventional

The purpose of this prospective randomized controlled trial was to compare intensive insulin therapy with a carbohydrate restrictive strategy in patients with acute ischemic stroke evaluating the outcome through the Glasgow Outcome Scale Extended, hospital mortality and NIHSS during the ICU stay.

NCT ID: NCT00744315 Unknown status - Clinical trials for Ischemic Cardiopathy

Induced Angiogenesis by Genic Therapy in Advanced Ischemic Cardiomyopathy

THEANGIOGEN
Start date: November 2007
Phase: Phase 2
Study type: Interventional

Human Vascular Endothelial Grown Factor 165 (hVEGF165) administration is promising therapy induces a new vessels, arterioles and capillaries in regions whose revascularization surgery is not possible by direct or by percutaneous angioplasty. This study aims to evaluate the clinical effects and safety of gene therapy with hVEGF165 in patients with advanced coronary artery disease.

NCT ID: NCT00743769 Withdrawn - Clinical trials for Myocardial Infarction

A Phase 1 Safety Study of the Intravenous Administration of Thymosin Beta in Healthy Volunteers

Start date: April 2008
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine whether the intravenous administration of single- and multiple-ascending doses of Thymosin Beta 4 is safe and tolerable in healthy volunteers.

NCT ID: NCT00743236 Completed - Kidney Cancer Clinical Trials

Warm Ischemia or Cold Ischemia During Surgery in Treating Patients With Stage I Kidney Cancer

Start date: August 2008
Phase: N/A
Study type: Interventional

RATIONALE: Warm ischemia is the clamping of blood vessels without cooling the kidney. Cold ischemia is the clamping of blood vessels with kidney cooling. It is not yet known whether warm ischemia is more effective than cold ischemia in patients undergoing surgery for stage I kidney cancer. PURPOSE: This randomized phase III trial is studying warm ischemia to see how well it works compared with cold ischemia during surgery in treating patients with stage I kidney cancer.