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Ischemia clinical trials

View clinical trials related to Ischemia.

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NCT ID: NCT00696124 Completed - Clinical trials for Critical Limb Ischemia

Safety Study of Gene Therapy in Treating Lower Leg Ischemia

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

The purpose of this study is to determine the safety, tolerability and preliminary efficacy of intramuscular injections of VM202 for subjects with critical limb ischemia. Subjects selected for this study will have critical limb ischemia that has not responded to standard therapy with symptoms including pain at rest and/or ischemic ulcers.

NCT ID: NCT00694395 Completed - Clinical trials for Acute Ischemic Stroke

A Qualitative Study of Delays in Hospital Admission in Patient With Acute Stroke

Start date: August 2006
Phase: N/A
Study type: Observational

To identify the circumstance during decision making processes to seek medical help in patients with symptoms of acute ischemic stroke.

NCT ID: NCT00691613 Not yet recruiting - Clinical trials for Myocardial Infarction

Infusion of a Single Dose of Erythropoietin to Prevent Injury in an Ischemia Reperfusion Forearm Model

IPIIR
Start date: July 2010
Phase: N/A
Study type: Interventional

Rationale: The investigators hypothesize that EPO protects against apoptosis after acute ischemia in man and that it is detectable using the annexin-A5 model. Objective: Does infusion of a single dose of Epoetin Alfa, a short-acting EPO, protect against apoptosis in man after acute ischemia? Study design: A double blinded randomised cross-over study. Study population: 12 Healthy male volunteers, between 18 and 40 years old. Intervention: All 12 volunteers will receive a single dose of EPO and placebo in a randomized order. A six week wash-out period is obtained in order to avoid interference of both treatments. Main study parameters/endpoints: The percentage of difference between radioactivity (quantified as counts per pixel) of the experimental and control thenar muscle at one and four hours after reperfusion.

NCT ID: NCT00690209 Completed - Clinical trials for Ischemic Heart Disease

By Pass Surgery With Stem Cell Therapy in Chronic Ischemic Cardiopathy

Start date: May 2008
Phase: Phase 2
Study type: Interventional

Surgical revascularization has proven its efficacy in term of morbidity and mortality in patients with multivessel coronary disease and poor left ventricular function. Nevertheless, if left ventricle is severely dilated, the improvement of global contractility and reduction of volumes is frequently absent after CABG even if substantial amount of myocardial viability is present. A value of > 140 ml for end systolic volume has been proposed as the cut off for the absence of recovery after revascularization. Recently, a reduction of cardiac volumes and improvement of regional and global contractility has been demonstrated in patients with advanced ischemic heart disease, severe dilation of left ventricle and poor candidates for revascularization after injection of stem cells in territories with residual viability.

NCT ID: NCT00682565 Completed - Heart Failure Clinical Trials

PK and Tolerability of IV and Oral CK-1827452 in Patients With Ischemic Cardiomyopathy and Angina

Start date: April 2008
Phase: Phase 2
Study type: Interventional

This study investigates whether symptom-limited exercise capacity in ischemic cardiomyopathy patients with angina is deleteriously affected by treatment with CK-1827452.

NCT ID: NCT00677404 Completed - Ischemia Clinical Trials

Autologous Transplantation of Bone Marrow Mononuclear Cell (BM-MNC) With and Without Granulocyte-Colony Stimulation Factor (G-CSF) for Treatment of Chronic Lower Limb Ischemic Patients

Start date: January 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to investigate the efficacy and safety of autologous transplantation of mononuclear cells with and without G-CSF in patients with chronic lower limb ischemia.

NCT ID: NCT00671203 Completed - Aortic Aneurysm Clinical Trials

Prevention of Colon Ischemia During Aortic Aneurysm (AAA) Repair

Start date: June 2007
Phase: Phase 3
Study type: Interventional

Patients undergoing surgery on their Aorta can get ischemia, a lack of blood flow, to their intestines and colon. This is very serious, as 2 out of 3 patients who have this problem die before leaving the hospital. A device developed by Spectros, called T-Stat, is approved by the US FDA to detect ischemia, and has been reported to detect ischemia in AAA aneurysm surgery and stenting, allowing the surgeon or interventional radiologist to take action quickly, while the colon ischemia is still treatable. This purpose of this study is to establish how T-Stat can best be used to prevent deaths.

NCT ID: NCT00669552 Completed - Ischemia Clinical Trials

Intracardiac T-wave Alternans and Ischemia

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

T-wave alternans is a test that looks at microvolt changes in the T-wave on a beat to beat basis. The presence or absence of such changes has been shown to predict or exclude future arrhythmic events. The mechanism of T-wave alternans is unclear, but may relate to calcium metabolism in the heart, and may be affected by conditions such as ischemia or heart failure. The purpose of this study is to determine whether T-wave alternans, as measured through the lead of an implantable defibrillator, is produced by acute ischemia induced by occlusion during percutaneous coronary interventions.

NCT ID: NCT00665028 Completed - Myocardial Ischemia Clinical Trials

Perioperative Ischemia Reduction Study (PROSE) Pilot

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

After surgery, patients who have cardiogram changes consistent with a lack of oxygen to the heart muscles, also known as myocardial ischemia, have been found to have 9 times the chance of having an event such as a heart attack during the subsequent 30 days. It is not known if monitoring and treating ischemia will prevent events such as heart attacks. It is not known if such monitoring and treatment can be done on the regular surgical wards. In this pilot study, we hope to demonstrate that such a study is feasible, and the maintenance of blinding is possible. The primary outcomes are to show that such monitoring after surgery is possible in ≥ 95% of patients, to show that response and treatment to such ischemia in ≤ 1 hour is possible in ≥ 90% of patients, and that blinding between the standard and active treatment groups is possible for 50% ± 1 s.d.. With the pilot study data, if successful, we will be applying for peer-reviewed funding for a full study.

NCT ID: NCT00661323 Completed - Clinical trials for Myocardial Infarction

Evaluating a New Echocardiography Imaging Procedure for Evaluating Heart Function

Start date: July 2010
Phase:
Study type: Observational

Magnetic resonance imaging (MRI) and echocardiography are two imaging methods that are used to obtain pictures of the heart and assess heart function. This study will evaluate a new, four-dimensional echocardiography approach of obtaining heart images to determine if it is as effective at evaluating heart function as MRI.