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Myocardial Injury clinical trials

View clinical trials related to Myocardial Injury.

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NCT ID: NCT01903161 Completed - Myocardial Injury Clinical Trials

Effect of Delayed Remote Ischemic Preconditioning on Myocardial Injury

RIPC
Start date: May 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate delayed myocardial protective effect of RIPC in patients undergoing cardiac valve replacement surgery.

NCT ID: NCT01688648 Completed - Arrhythmia Clinical Trials

Comparison Between Lidocaine, Dexmedetomidine, and Their Combined Infusion in Subjects Undergoing Coronary Artery Bypass Graft

Start date: September 2012
Phase: N/A
Study type: Interventional

The aim of the present study is to compare the antiarrhythmic and myocardial protective effect between lidocaine, dexmedetomidine, and their combined infusion in subjects undergoing coronary artery bypass graft.

NCT ID: NCT01406678 Completed - Myocardial Injury Clinical Trials

Remote Ischemic Preconditioning in Coronary Artery Bypass Grafting With Cold Crystalloid Cardioplegic Arrest

Start date: July 2008
Phase: Phase 2/Phase 3
Study type: Interventional

Remote ischemic preconditioning (RIPC) with transient upper limb ischemia/reperfusion reduces myocardial injury in patients undergoing on-pump coronary artery bypass (CABG) surgery with cross-clamp fibrillation or blood cardioplegia for myocardial protection. The present study assesses protection of heart, brain and kidney by RIPC under crystalloid cardioplegic arrest. The study also addresses safety and clinical outcome.

NCT ID: NCT01308138 Completed - Myocardial Injury Clinical Trials

Myocardial Physiology And Microanatomy In Individuals Undergoing Heart Surgery

TRIMRIPC
Start date: January 2011
Phase: N/A
Study type: Interventional

The main focus of the project is to determine to what degree myocardial energy metabolism is linked to impaired function in human cardiomyocytes, whether exercise training and remote ischemic preconditioning can restore cardiomyocyte function and whether this is linked to improved mitochondrial and cell function.

NCT ID: NCT01260259 Completed - Acute Kidney Injury Clinical Trials

Seattle Cardiorenal Remote Ischemic Preconditioning Trial

SCRIPT
Start date: December 2010
Phase: N/A
Study type: Interventional

Remote Ischemic Preconditioning (RIPC) is a treatment that may be associated with improved outcomes after cardiac surgery. It can be elicited noninvasively by using a tourniquet to elicit transient ischemia over a lower extremity. It is thought to promote anti-inflammatory and cell survival pathways, and thus protect remote organs against future ischemic injury. We hypothesize that compared to sham treatment, RIPC will be associated with decreased post-operative acute kidney, myocardial, and lung injury.

NCT ID: NCT00817791 Completed - Brain Injury Clinical Trials

Preconditioning With Hyperbaric Oxygen in Cardiovascular Surgery

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

Animal studies have shown that preconditioning with hyperbaric oxygen can induce central nervous system and heart ischemic tolerance. This study was designed to determine the protective effect of hyperbaric oxygen preconditioning on brain and myocardium ischemia-reperfusion injury during coronary artery bypass graft surgery.

NCT ID: NCT00734383 Completed - Myocardial Injury Clinical Trials

Propofol Cardioprotection for Type II Diabetics

Start date: April 2005
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine if an intravenous anesthetic with antioxidant properties will protect the heart of diabetic patients from injury while undergoing coronary bypass surgery.

NCT ID: NCT00569816 Completed - Myocardial Injury Clinical Trials

Continuous Versus Repetitive Sevoflurane Administration for Preconditioning

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

Pharmacologic preconditioning by volatile anesthetics may depend on the mode of administration. The researchers hypothesize that a continuous administration in patients scheduled for CABG surgery prebypass will be less effective in terms of attenuating myocardial cell damage compared to a repetitive administration with a double wash in/wash out schedule. A control group will receive propofol as their primary anesthetic.

NCT ID: NCT00007358 Completed - Myocardial Injury Clinical Trials

Dexamethasone Treatment for Congenital Heart Block (CHB) in Newborns With Lupus

Start date: October 2000
Phase: N/A
Study type: Interventional

Some newborns are born with congenital heart block (CHB), a condition occurring in babies with neonatal lupus. The first part of the study will test the effectiveness of fluorinated steroids, including dexamethasone, in improving the heart function and general health of newborns who have auto-antibody-associated CHB. The second part of this study will use ultrasound and heart monitoring to observe high-risk pregnant women and their fetuses during the third trimester of pregnancy.