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Reperfusion Injury clinical trials

View clinical trials related to Reperfusion Injury.

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NCT ID: NCT00402506 Completed - Myocardial Ischemia Clinical Trials

A Safety and Efficacy Study to Confirm the Cardioprotective Effects of MC-1 in Patients Undergoing High-Risk CABG

Start date: November 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the effect of MC-1 on the combined incidence of cardiovascular death and nonfatal myocardial infarction (MI) up to and including 30 days following coronary artery bypass graft (CABG) surgery compared with placebo.

NCT ID: NCT00385151 Completed - Clinical trials for Endothelial Dysfunction

To Compare the Ischemic Pre-conditioning and Post-conditioning on Reperfusion Injury in Humans.

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

Reperfusion Injury occurs by the sudden blood flow to the injured and ischemic myocardium during restoration of blood flow either by Mechanical revascularization or thrombolysis. A phenomenon known as Pre-conditioning has been identified to limit the the extent and severity of reperfusion injury but it is very difficult to apply it in patient care setting as timing of acute cardiac or neurologic ischemic event is difficult to reliably predict. Postconditioning or ischemic postconditioning is well known to attenuate the reperfusion injury. There is enough data that shows the benefit of post conditioning in reducing the reperfusion injury in animals. However postconditioning in humans has not been investigated. We hypothesize that Post conditioning will attenuate the reperfusion injury and will be comparable to the effect of preconditioning in humans.

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: NCT00286312 Completed - Clinical trials for Myocardial Infarction

Myocardial Infarction Size Reduction With Atorvastatin

Start date: February 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if oral atorvastatin administered just before percutaneous coronary angioplasty for acute myocardial infarction improves early and late heart function as compared to placebo.

NCT ID: NCT00265239 Completed - Clinical trials for Myocardial Infarction

Pilot Study of Edaravone to Treat Acute Myocardial Infarction

Start date: April 2001
Phase: Phase 4
Study type: Interventional

Early reperfusion therapy has improved the clinical outcomes of patients with acute myocardial infarction (AMI), but these benefits are limited in some patients by reperfusion injuries. There is now increasing evidence that reactive oxygen species cause reperfusion injury. This study was designed to examine the effects of edaravone, a novel free radical scavenger, in patients with AMI.

NCT ID: NCT00248040 Completed - Kidney Diseases Clinical Trials

Reparixin in Prevention of Delayed Graft Function After Kidney Transplantation

Start date: October 2005
Phase: Phase 2
Study type: Interventional

The chemokine CXCL8 plays a key role in the recruitment and activation of polymorphonuclear neutrophils in post-ischemia reperfusion injury after solid organ transplantation. Reparixin is a novel, specific inhibitor of CXCL8. This study is configured to explore the safety and efficacy of reparixin in preventing the delayed graft function (DGF) after kidney transplantation.

NCT ID: NCT00246740 Completed - Clinical trials for Cardiopulmonary Bypass

Protection of the Heart With Doxycycline During Coronary Artery Bypass Grafting

Start date: October 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether doxycycline (Periostat) at a sub-antimicrobial dose will decrease reperfusion injury after coronary artery bypass grafting (CABG) surgery with cardiopulmonary bypass (CPB).

NCT ID: NCT00229047 Completed - Ischemia Clinical Trials

Ischemia and Reperfusion Injury in the Human: An Observational Study

Start date: April 2005
Phase: N/A
Study type: Observational

We, the researchers at Lawson Health Research Institute, propose to investigate the impact of surgical ischemia and reperfusion on skeletal muscle microcirculation using a hand-held microscope.

NCT ID: NCT00226369 Completed - Clinical trials for Congenital Heart Defects

Cylexin for Reduction of Reperfusion Injury in Infant Heart Surgery

Start date: December 1997
Phase: Phase 2/Phase 3
Study type: Interventional

We conducted a multicenter, randomized, placebo-controlled trial of Cylexin, an inhibitor of the attachment of white blood cells to the endothelium. Our study population was neonates and infants undergoing hypothermic cardiopulmonary bypass during surgical repair or palliation of congenital heart defects.

NCT ID: NCT00224406 Completed - Clinical trials for Lung Transplantation

Repertaxin in Prevention of Primary Graft Dysfunction After Lung Transplantation

Start date: May 2005
Phase: Phase 2
Study type: Interventional

The chemokine CXCL8 plays a key role in the recruitment and activation of polymorphonuclear neutrophils in post-ischemia reperfusion injury after solid organ transplantation. Repertaxin is a novel, specific inhibitor of CXCL8. This study is configured to explore the safety and efficacy of repertaxin in preventing the primary graft dysfunction (PGD) after lung transplantation.