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Ischemia clinical trials

View clinical trials related to Ischemia.

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NCT ID: NCT00371371 Completed - Ischemia Clinical Trials

Intra-arterial Stem Cell Therapy for Patients With Chronic Limb Ischemia (CLI)

JUVENTAS
Start date: September 2006
Phase: Phase 1/Phase 2
Study type: Interventional

The purposes of this study are to determine whether intra-arterial injection of autologous stem cells is effective in the treatment of chronic limb ischemia (CLI), to characterize stem cell dysfunction in patients with CLI, and to relate the stem cell function with clinical outcome.

NCT ID: NCT00368628 Completed - Clinical trials for Acute Ischemic Stroke

Continuous Positive Airway Pressure for the Treatment of Stroke

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

New stroke therapies are needed. This study seeks to provide the preliminary data needed to plan a future study that will evaluate the efficacy of using continuous positive airway pressure (CPAP) to treat stroke patients who have sleep apnea. Our goal is to use this therapy to reduce stroke symptom severity.

NCT ID: NCT00360386 Completed - Ischemia Clinical Trials

ALBION "Assessment of the Best Loading Dose of Clopidogrel to Blunt Platelet Activation, Inflammation and Ongoing Necrosis"

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

- To compare the Kinetics of inhibition of platelet aggregation (aggregometry) and platelet activation (flow cytometry) with different loading doses of clopidogrel - To evaluate the effect on various parameters of inflammation and necrosis and the safety of these loading doses

NCT ID: NCT00355147 Completed - Ischemic Stroke Clinical Trials

Adapting Tools to Implement Stroke Risk Management to Veterans

TOOLS
Start date: January 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to develop and evaluate the local adaptation of existing stroke prevention tools into practice. A stroke prevention program is a collection of materials including written materials like pamphlets and brochures, videotapes and training guides for stroke survivors and evidence based guidelines for the doctors that provide care for them. Other tools that may be used in a stroke prevention program include devices that help patients monitor medical symptoms at home like home blood pressure machines or blood sugar monitors and messaging devices that allow reporting symptoms from home to a health care provider. We hypothesized Veterans with stroke who receive the Veteran Stroke Prevention Program would engage in better medication compliance and stroke specific quality of life compared to those who did not receive the program.

NCT ID: NCT00328640 Completed - Ischemic Stroke Clinical Trials

Quality Improvement in Stroke Prevention (QUISP)

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

Is a secondary prevention intervention, focused on implementation of standardized pre-printed discharge orders for hospitalists, effective at increasing utilization of the following evidence-based treatments 6 months after discharge for ischemic stroke: 1. Treatment with statins, 2. Control of hypertension, and 3. Anticoagulation in patients with atrial fibrillation.

NCT ID: NCT00326976 Completed - Clinical trials for Myocardial Infarction

Efficacy of FX06 in the Prevention of Myocardial Reperfusion Injury

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

The purpose of the study is to evaluate whether FX06 is capable of limiting infarct size following balloon catheterization for acute myocardial infarction.

NCT ID: NCT00321022 Completed - Clinical trials for Transient Ischemic Attack

Transient Ischemic Attack (TIA) Accelerated Diagnostic Protocol

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

The primary objective of this study is to determine if emergency department patients with Transient Ischemic Attack (TIA) that are managed using a TIA "accelerated diagnostic protocol", or "ADP", demonstrate a significant decrease in their index visit length of stay and cost, with comparable diagnostic and 90-day clinical outcomes relative to TIA patients randomized to traditional inpatient care. The secondary objectives are to evaluate the potential role of a TIA risk stratification tool and to determine the time to a diagnostic endpoint in both groups.

NCT ID: NCT00315510 Completed - Ischemia Clinical Trials

Rosuvastatin and Ischemia Reperfusion

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

Statins, including rosuvastatin, are drugs that lower plasma cholesterol and prevent atherosclerotic disease. Recent preclinical evidence suggests that statins also increase tissue tolerance to ischemia-reperfusion injury. This is a randomized, double blind, parallel designed study comparing the effect of 1 week treatment with rosuvastatin (20 mg, once a day) with placebo on forearm ischemia-reperfusion injury in healthy male volunteers. Forearm ischemia-reperfusion injury is quantified with Tc-99m-annexin A5 scintigraphy of the hands after a standardized ischemic exercise test. For this purpose, Tc-99m-rh-annexin A5 (400 MBq; < 5 mSv) is injected intravenously upon reperfusion, followed by scintigraphy of both hands with a gamma camera at 1 and 4 hours after injection. Annexin A5 targeting is calculated as the percentage difference in activity (counts/pixel) between the thenar muscles of both hands.

NCT ID: NCT00304837 Completed - Clinical trials for Critical Limb Ischemia

VEGF Gene Transfer for Critical Limb Ischemia

Start date: n/a
Phase: Phase 1
Study type: Interventional

The purpose of this gene therapy study is to evaluate the safety and efficacy of intramuscular gene transfer using Vascular Endothelial Growth Factor (VEGF) or placebo in patients with moderate to high-risk Critical Limb Ischemia (a condition in which there is poor blood circulation in the leg). This trial will assess whether VEGF improves rest pain and/or heals ulcers in the legs of patients with peripheral artery disease (blockages in leg arteries.) VEGF is DNA, or genetic material that will be injected into the leg muscles on three separate occasions, each 2 weeks apart. Once the DNA is in the leg, it directs the cells of the artery wall to increase its production of VEGF, which has been shown to cause new blood vessels to grow. This experimental therapy is designed to grow new blood vessels around blockages in the leg arteries. The total length of participation in this study is approximately 1 year and will require approximately 8 clinic visits within that year. Following enrollment in the study, testing may be done for cancer screening, blood work, physical exams, vascular testing and eye exams. There is no charge for any testing or office visits required by the study. This study has been approved by the Food and Drug Administration (FDA).

NCT ID: NCT00300053 Completed - Myocardial Ischemia Clinical Trials

ACT34-CMI -- Adult Autologous CD34+ Cells

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

The purpose of this study is to evaluate the efficacy and safety of intramyocardial injections of CLBS14 in patients with refractory chronic myocardial ischemia.