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Reperfusion Injury clinical trials

View clinical trials related to Reperfusion Injury.

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NCT ID: NCT01208727 Completed - Clinical trials for Myocardial Reperfusion Injury

Post Cond No Reflow

Start date: April 2009
Phase: N/A
Study type: Interventional

After having shown that postconditioning allowed a significant 36% reduction of infarct size as assessed by blood levels of myocardial enzymes in acute myocardial patients, the investigators objective is to assess the effect of postconditioning in acute myocardial infarction (AMI) patients on microvascular obstruction lesions defined by cardiac MRI images.

NCT ID: NCT01172171 Completed - Clinical trials for Acute Myocardial Infarction

The Effect of Melatonin on Ischemia-reperfusion Injury Following Acute Myocardial Infarction

Start date: June 2013
Phase: Phase 2
Study type: Interventional

In Denmark, 12.000 people a year, is struck by acute myocardial infarction. A third of these cannot be saved before treatment is possible. Despite quick and effective reperfusion of the coronary arteries using PCI (Percutaneous Coronary Intervention) after an acute ST-elevation myocardial infarction, substantial morbidity and mortality remain. Infarct size is an important determinant of the short-and long-term outcome after acute myocardial infarction. The most widely used and most effective proven therapy to limit infarct size is the early reperfusion induced by or PCI. Although beneficial in terms of myocardial salvage, reperfusion itself may contribute to additional damage of the myocardium; the damage due to the combined processes is known as "ischemia-reperfusion injury". The pathogenesis of myocardial ischemia-reperfusion injury is a multifactorial process involving the interaction of multiple mechanisms. Numerous studies indicate that there are three pivotal factors in the pathogenesis of ischemia-reperfusion injury: elevated oxidative damage, depressed energy metabolism, and altered calcium homeostasis. Partially reduced species of oxygen, including the superoxide anion radical, hydroxyl radical, and hydrogen peroxide, are generated intracellularly as by-product of oxygen metabolism. These reactive oxygen species cause peroxidation af membrane lipids, denaturation of proteins, and modification of DNA, all of which ultimately can lead to cell death. In mammals, cell damage induced by partially reduced oxygen species can also initiate local inflammatory responses, which then lead to further oxidant-mediated tissue injury. Melatonin is mainly known for its role as an endogenously produced circadian hormone. For the last twenty years, increasing evidence has proven melatonin to be a very potent direct and indirect antioxidant. Recent experimental studies have documented the beneficial effects of melatonin in reducing tissue damage and limiting cardiac pathophysiology in models of experimental ischemia-reperfusion. Primary hypothesis: Melatonin given to patients undergoing PCI can reduce the myocardial damage sustained by ischemia-reperfusion.

NCT ID: NCT01167569 Completed - Reperfusion Injury Clinical Trials

Study of High Dose Vitamin C On Outcome in Cardiac Surgery Patients

VitaminC
Start date: October 2007
Phase: Phase 4
Study type: Interventional

It has been shown that the stress that occurs during cardiac surgery leads to early decrease of many of the body's resources such as Vitamin C (ascorbic acid) which may contribute to complications after surgery. This study will investigate the effects of high doses of intravenous (IV) Vitamin C on the outcome and complications after cardiac surgery.

NCT ID: NCT01144585 Completed - Acute Lung Injury Clinical Trials

Effects of Remote Ischemic Preconditioning and Postconditioning on Lung Injury During Cardiopulmonary Bypass

Start date: May 2010
Phase: N/A
Study type: Interventional

Remote Ischemic Preconditioning(RIPC) and remote ischemic postconditioning(RIPoC) seems to have a protective effect during ischemic period. Using cardiopulmonary bypass(CPB) during open heart surgery reduces pulmonary blood flow and may cause ischemic damage to lung tissue. The investigators anticipate that RIPC and RIPoC may reduce lung injury after CPB.

NCT ID: NCT01113008 Completed - Clinical trials for Myocardial Reperfusion Injury

Remote Ischemic Postconditioning in Humans

Start date: February 2009
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the phenomenon of remote ischemic post-conditioning in humans. The minor myocardial damage associated with percutaneous revascularization procedures may be attenuated by producing controlled ischemia in the arms immediately after carrying out these procedures (remote ischemic post-conditioning). The justification and design of this clinical trial has been reported: Cardiology. 2011;119(3):164-9.

NCT ID: NCT01073202 Completed - Clinical trials for Liver Transplantation

Effects of Ursodeoxycholic Acid on Graft Recovery Early After Adult Liver Transplantation

Start date: May 2005
Phase: N/A
Study type: Interventional

This study is designed to investigate the possible beneficial effects of UDCA on liver graft recovery early after adult liver transplantation.

NCT ID: NCT01040013 Completed - Laparoscopy Clinical Trials

Gut Oxygenation and Laparoscopy

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

Patients with left-colon cancer will be randomized to laparoscopic or laparotomic operation. during surgery and for 6 days after operation, intestinal oxygen tension and ischemia-reperfusion injury markers will be evaluated to understand if pneumoperitoneum is associated with reduced splanchnic blood flow and ischemia-reperfusion injury.

NCT ID: NCT01004289 Completed - Clinical trials for Myocardial Reperfusion Injury

POSTconditioning During Coronary Angioplasty in Acute Myocardial Infarction Study

POST-AMI
Start date: April 2007
Phase: Phase 2
Study type: Interventional

The POST-conditioning during coronary angioplasty in Acute Myocardial Infarction (POST-AMI) trial will evaluate the usefulness of postconditioning in limiting infarct size and microvascular damage during the early and late phases after AMI.

NCT ID: NCT00995670 Completed - Hyperglycemia Clinical Trials

Ischemia/Reperfusion Injury of Human Endothelium: Role of Glucose and Statins

Start date: March 2010
Phase: N/A
Study type: Interventional

Anesthetic preconditioning (APC, a brief exposure to an anesthetic gas) has become an area of intense research interest because of its ability to protect tissue and organs from injury resulting from a cessation of blood flow and then a re-establishment of flow. The blood vessel lining plays a key role in this injury. This research will examine, in human volunteers, several important modifiers of APC in human blood vessels: high blood sugar, vitamin C, and statin drugs. Thus, the proposed studies will advance the investigators' understanding of mechanisms of this injury in humans and explore important modifiers of APC protection from injury.

NCT ID: NCT00994981 Completed - Reperfusion Injury Clinical Trials

Magnesium Administration in Liver Transplantation and Reperfusion Injury

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

The purpose of this study is to evaluate the effect of intravenous magnesium infusion before reperfusion with employing some clinical parameters including blood lactate levels, because the intraoperative changes in the blood lactate levels after hepatic allograft reperfusion served as an accurate predictor of the initial graft function in living donor liver transplantation.