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Cardiac Surgical Procedures clinical trials

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NCT ID: NCT01029314 Completed - Clinical trials for Cardiac Surgical Procedures

Pilot Study of the Genius(TM)2 Tympanic Thermometer in Cardiac Patients Requiring Cardiopulmonary Bypass

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

Primary study objective is to test the accuracy of the Genius 2 tympanic thermometer and the Exergen TAT-5000(TM) temporal artery thermometer as compared with serial perioperative core temperature measurements obtained in cardiac surgical patients during cardiopulmonary bypass. Study hypothesis: The Genius 2 thermometer will display greater precision and accuracy than the Exergen TAT-5000 thermometer when compared to core body temperature in patients undergoing CABG surgery.

NCT ID: NCT00997217 Completed - Clinical trials for Cardiac Surgical Procedures

The Effect of Remote Ischemic Preconditioning in the Cardiac Surgery

RIPC
Start date: October 2009
Phase: Phase 1
Study type: Interventional

Perioperative myocardial injury is a serious complication of cardiac surgery. This complication increases both mortality and morbidity of cardiac surgery. Remote ischemic preconditioning (RIPC) is the concept that brief ischemia followed by reperfusion in an organ can reduce subsequent ischemia-reperfusion injury in distant organs. Recent several clinical trials showed powerful myocardial protective effect of remote ischemic preconditioning by reducing postoperative cardiac enzymes. However, the evidence that remote ischemic preconditioning can improve the clinical outcomes such as mortality and morbidity, is still lacking. The investigators perform a multicenter randomized controlled study to evaluate that remote ischemic preconditioning can improve the outcomes of cardiac surgery.

NCT ID: NCT00990795 Terminated - Clinical trials for Cardiac Surgical Procedures

Trial of Cyclosporine for Myocardial Protection During Open Heart Surgery

CYCLO1
Start date: April 2010
Phase: Phase 1
Study type: Interventional

Administration of cyclosporine has been found to have a myocardial protective effect, improving post-operative cardiac function in patients undergoing percutaneous coronary interventions by diminishing infarct size. The purpose of the proposed study is to conduct a randomized, controlled clinical trial in patients undergoing isolated valvular heart surgery, or coronary artery bypass surgery. Specifically the investigators will evaluate the cardio-protective effects of cyclosporine on post ischemic-arrest myocardium. The two factors will be treatment group and cyclosporine versus placebo.

NCT ID: NCT00881686 Completed - Clinical trials for Heart Defects, Congenital

Myocardial Protection With Adenosine Preconditioning

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

Adenosine has been proved to be an important mediator of myocardial protection induced by ischemic preconditioning. The hypothesis of this study is that adenosine preconditioning can provide additional myocardial protection in the setting of pediatric open heart surgery with cardioplegia and cardiopulmonary bypass.

NCT ID: NCT00577434 Terminated - Clinical trials for Cardiac Surgical Procedures

Pharmacokinetics and Pharmacodynamics of Pentobarbital in Neonates, Infants, and Children Following Open Heart Surgery

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

This medication is used for procedural sedation and sedation for diagnostic imaging. The purpose of this study is to find out what happens to pentobarbital in the body after it is given to children who have had heart surgery.

NCT ID: NCT00512161 Completed - Clinical trials for Cardiac Surgical Procedures

Placement of Permanent Pacemaker Study

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

The purpose of this study is to determine the predictors for placement of permanent pacemakers soon after cardiac surgery. We will measure the following to see what influence, if any, they have on predicting the need for permanent pacemaker implantation. 1. Type of cardiac surgery 2. Gender of patient 3. Patient's age 4. Preoperative heart rhythm and rate 5. Duration on cardiopulmonary bypass 6. Immediate post cardiopulmonary bypass heart rhythm and rate. 7. All heart rhythms and rates identified in the postoperative period prior to permanent pacemaker implantation. 8. Underlying heart rhythm and rates when permanent pacemaker is placed. 9. Ejection fraction before surgery 10. Ejection fraction immediately post-cardiopulmonary bypass

NCT ID: NCT00500981 Completed - Clinical trials for Cardiac Surgical Procedures

Internal Jugular Vein Ultrasound Measures and Fluid Responsiveness in Post-Operative Cardiac Surgical Patients

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

The goal of this study is to evaluate whether measures of the size of the internal jugular vein have clinical utility in predicting whether patients may benefit from treatment with intravenous fluid.

NCT ID: NCT00459082 Completed - Clinical trials for Cardiac Surgical Procedures

A Pharmacokinetic Study of Dexmedetomine in Infants

Start date: May 2004
Phase: Phase 1
Study type: Interventional

Blind randomized trial of a single bolus dose of dexmedetomine followed by a continuous infusion (CIVI) for up to 24 hours in infants who immediately post-operative from cardiac surgery and require tracheal intubation with mechanical ventilation in the post-operative period. Three bolus and infusion dose will be administered to a total of 36 patients.

NCT ID: NCT00427388 Active, not recruiting - Clinical trials for Cardiopulmonary Bypass

Steroids In caRdiac Surgery Trial (SIRS Trial)

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

SIRS trial is a large simple study in which high-risk patients undergoing cardiac surgery requiring the use of cardiopulmonary bypass (CPB) are randomly allocated to receive a pulse dose of Methylprednisolone or a matching placebo. Cardiopulmonary bypass initiates a systemic inflammatory response that facilitates development of post-operative complications. SIRS will confirm or deny the potential clinical benefits of suppressing this response through the use of systemic steroids. Specifically, does 250 mg of intravenous Methylprednisolone given twice, once on anesthetic induction and again on CPB initiation, result in improved early survival and less myocardial infarction in high-risk cardiac surgery patients requiring CPB?

NCT ID: NCT00359398 Terminated - Clinical trials for Cardiopulmonary Bypass

Sequestration of Platelets Prior to Bypass Reduces Bleeding After Cardiac Surgery

Start date: August 2006
Phase: Phase 2
Study type: Interventional

Excessive bleeding is common after cardiac surgery. This may result in patients receiving a blood transfusion or suffering the life-threatening complication of cardiac tamponade. Tamponade is when excessive bleeding compresses the heart and prevents it from pumping properly. A major reason for the bleeding is the damage done to platelets by the cardiopulmonary bypass (CPB) machine. Often patients receive platelets and plasma from blood donors to try to reduce the bleeding post-operatively. The investigators plan to take platelets and plasma from patients before they are damaged. They would then return these 'undamaged' sequestered platelets to the patients after the bypass machine is no longer needed. Therefore, the investigators' primary question is whether platelet sequestration would reduce the bleeding problems that occur following cardiac surgery. They will evaluate bleeding problems using thromboelastography, which provides a comprehensive assessment of both how blood clots form and their strength. If sequestration reduces bleeding problems following cardiac surgery then it may reduce the chance of patients receiving blood products from donors. Although donated blood is thoroughly tested, its use does expose patients to the risk of transfusion errors, blood borne infections and reactions. Avoiding its use would be very desirable.