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Reperfusion Injury clinical trials

View clinical trials related to Reperfusion Injury.

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NCT ID: NCT01857414 Active, not recruiting - Clinical trials for Myocardial Reperfusion Injury

Effect of RIC on Clinical Outcomes in STEMI Patients Undergoing pPCI

CONDI2
Start date: November 2013
Phase: N/A
Study type: Interventional

The aim of the the study is to investigate whether Remote Ischaemic Conditioning (RIC) can improve clinical outcomes (cardiac death and hospitalisation for heart failure) at one year in patients presenting with ST-elevation Myocardial Infarction and undergoing primary percutaneous coronary intervention. This will be done in a multinational investigator-driven, multi-centre, randomised, controlled, single-blind, parallel assignment, prospective clinical efficacy trial.

NCT ID: NCT01771978 Active, not recruiting - Clinical trials for Ischaemia-reperfusion Injury

Ischaemia-réperfusion During the Coronary Surgery With Beating Heart

Start date: June 2002
Phase: Phase 3
Study type: Interventional

Less oxidative stress occurs during off-pump than on-pump coronary artery bypass graft (CABG) surgery but warm ischaemia-reperfusion injury may occur following transient coronary artery clamping. The aim of this study was to compare the preventive effects of diltiazem and N-acetylcysteine (NAC), alone or in combination, on biomarkers of myocardial damage and oxidative stress during off-pump CABG surgery.

NCT ID: NCT01461512 Active, not recruiting - Clinical trials for Ischemia-reperfusion Injury

Heme Arginate in Functional Magnetic Resonance Imaging (fMRI)

Start date: January 2009
Phase: Phase 2
Study type: Interventional

Ischemia reperfusion injury may be attenuated by HO-1 induction. Heme arginate showed protective effects during prolonged ischemia in animal studies. Functional blood oxygen level dependent (BOLD) magnetic resonance imaging (MRI) shall evaluate the effects of HO-1 induction during short-time ischemia in skeletal muscle of healthy subjects.

NCT ID: NCT01172691 Active, not recruiting - Liver Transplant Clinical Trials

Trial of Inhaled Nitric Oxide (iNO) on Ischemia / Reperfusion Injury During Orthotopic Liver Transplantation With Marginal Grafts

Start date: July 2010
Phase: Phase 2
Study type: Interventional

This study is being done to determine if patients receiving (iNO) will have increased liver function and less damage from IR than patients who do not receive (iNO).

NCT ID: NCT00876902 Active, not recruiting - Clinical trials for Ischemia Reperfusion Injury

YSPSL for Prevention of Ischemic Reperfusion Injury in Patients Undergoing Cadaveric Orthotopic Liver Transplantation

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

The study is designed to assess the feasibility of evaluating YSPSL for the amelioration of ischemia reperfusion injury following liver transplantation by administering YSPSL into the liver graft directly ex vivo via the portal vein and to the recipient intravenously prior to reperfusion. This study is an extension of the recent pilot study YSPSL-0002 with an almost identical study protocol. The rationale of this and the previous study is based on the recent observation that P-selectin expression has been associated in liver grafts with prolonged cold storage times and rejection. By examining biomarkers of IRI including P-selectin by immunohistochemistry and/or quantitative PCR, liver histology and hepatic blood flow using established techniques, the goal of this study is to evaluate the feasibility of using these modalities for future studies of safety and efficacy.

NCT ID: NCT00204178 Active, not recruiting - Clinical trials for Kidney Transplantation

The Role of Reactive Oxygen Species in Ischaemia-Reperfusion Injury of the Transplanted Kidney

Start date: April 2003
Phase: N/A
Study type: Observational

Measurement of reactive oxygen species production and antioxidant system status before and directly after reperfusion of the transplanted kidney and influence of oxidant stress on kidney function in 2 and 6 weeks.

NCT ID: NCT00189007 Active, not recruiting - Reperfusion Injury Clinical Trials

Antenatal Allopurinol During Fetal Hypoxia

Start date: October 2009
Phase: Phase 3
Study type: Interventional

A former study (submitted) in 32 severely asphyxiated infants participating in a randomized double blind study, in which early postnatal allopurinol or a placebo (within 4 hours after birth) was administered to reduce free radical formation and consequently reperfusion/reoxygenation injury to the newborn brain, showed an unaltered high mortality and no clinically relevant improvement in morbidity in infants treated with allopurinol. It was hypothesized that postnatal allopurinol treatment started too late to reduce reperfusion-induced free radical surge and that initiating allopurinol treatment of the fetus with (imminent) hypoxia already via the mother during labor will be more effective to reduce free radical-induced post-asphyxial brain damage.