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Cardiopulmonary Bypass clinical trials

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NCT ID: NCT01248104 Completed - Clinical trials for Cardiopulmonary Bypass

Comparison of Tranexamic to Epsilon Aminocaproic Acid: a Prospective Analysis of Blood Conservation in Cardiac Surgery

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

We designed a prospective double-blinded randomized trial in an attempt to detect a difference between tranexamic acid (TXA) and epsilon aminocaproic acid (EACA) in reducing transfusion in patients undergoing cardiac surgery.

NCT ID: NCT01231776 Recruiting - Clinical trials for Heart Valve Diseases

Acupuncture Improves Sleep in Patients Undergoing Cardiopulmonary Bypass

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

Due to various causes, such as brain impairment, environment changes, anxious,et al. patients, who undergo cardiopulmonary bypass, often suffer from poor quality of sleep. In chinese traditional medicine, acupuncture can improve the quality of sleep in patients with sleeping disorder. But it remains acupuncture could improve the quality of sleep in patients with heart operations.

NCT ID: NCT01228305 Completed - Clinical trials for Congenital Heart Disease

Acetaminophen for Oxidative Stress After Cardiopulmonary Bypass

Start date: July 2011
Phase: N/A
Study type: Interventional

The current proposal tests the central hypothesis that acetaminophen will attenuate the oxidative stress response associated with cardiopulmonary bypass (CPB)-induced hemolysis in children undergoing cardiac surgery.

NCT ID: NCT01173822 Completed - Surgery Clinical Trials

Processed Residual Pump Blood in Cardiac Surgery: The PRBC Trial

PRBC
Start date: December 2004
Phase: N/A
Study type: Interventional

The study is an randomized controlled trial (RCT) of 198 coronary artery bypass graft (CABG) patients, exploring whether ultrafiltration of residual blood in the cardiopulmonary bypass circuit reduces transfusion and bleeding.

NCT ID: NCT01144039 Completed - Myocardial Ischemia Clinical Trials

Glutamate and Diastolic Function in Patients Undergoing Aortic Valve Repair

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

Purpose: The effect of intravenous glutamate infusion on myocardial diastolic function and overall hemodynamics were studied in patients undergoing elective aortic valve replacement with severe aortic stenosis and associated left ventricular hypertrophy . Methods: 25 patients will be included in this double-blind randomized placebo-controlled study. Glutamate was administered intravenously immediately after aortic cross-clamp release. The patients receive either a low dose of 30mg kg-1 h-1 (LG-group) or high dose of 60 mg kg-1 h-1 (HG-group) or placebo (P-group) at a rate of 3.3ml kg-1h-1 for 2h. Transesophageal echocardiography (TEE) is used to measure diastolic and systolic ventricular function before sternotomy (T0), and 2h (T2), 3h (T3) and 6h (T4) after release of cross clamp. Additionally routine hemodynamic parameters are measured intraoperatively.

NCT ID: NCT01022736 Completed - Clinical trials for Cardiopulmonary Bypass

Plasma Gabapentin Concentration During and Following Cardiac Bypass

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

This open label investigation is to determine whether cardiopulmonary bypass affects plasma gabapentin concentration after preoperative administration in the setting of cardiac bypass surgery. Following signed informed consent, 16 patients scheduled for cardiac bypass surgery will be given gabapentin (600mg, oral) 1 hour prior to surgery, 1 hour following extubation and then every 8 hours for a total of 4 doses. Plasma gabapentin levels will be measured prior to induction, prior to bypass, 10 min into the bypass procedure, 10 minutes before separation from bypass, 30 minutes following bypass and then before and 2 hours following each of the next 3 doses of gabapentin. Pain scores, sedation scores, side effects and morphine equivalents will be documented for one day following surgery.

NCT ID: NCT01002859 Terminated - Clinical trials for Cardiopulmonary Bypass

Effect of Preliminary Administration of Cyclosporine (Sandimmun ®) on Different Markers of Cardiac Ischaemia Induced by Cardiopulmonary Bypass

Ciclo et CEC
Start date: April 2009
Phase: Phase 2
Study type: Interventional

Observe the effect of preliminary cyclosporine administration on different markers of cardiac ischaemia led by the aortic cross-clamp during coronary artery bypass surgery with Cardiopulmonary bypass.

NCT ID: NCT00981474 Completed - Thoracic Surgery Clinical Trials

Cerebral Autoregulation Monitoring During Cardiac Surgery

Start date: September 1, 2009
Phase: N/A
Study type: Interventional

Neurological complications from cardiac surgery are an important source of operative mortality, prolonged hospitalization, health care expenditure, and impaired quality of life. New strategies of care are needed to avoid rising complications for the growing number of aged patients undergoing cardiac surgery. This study will evaluate novel methods for reducing brain injury during surgery from inadequate brain blood flow using techniques that could be widely employed.

NCT ID: NCT00906906 Recruiting - Clinical trials for Cardiopulmonary Bypass

Validation of Venous Cannulae Flow Ratings

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

The purpose of this study is to characterize blood flow in the plastic tubing of a heart-lung bypass machine during heart surgery. Technical specifications provided by the manufacturer do not consider varying hemodynamic conditions such as temperature and hemoglobin levels which affect blood viscosity and ultimately blood flow to and from the patient during heart-lung bypass. The investigator wishes to perform a prospective study of the heart-lung bypass tubing in children that require heart-lung bypass during heart surgery.

NCT ID: NCT00872001 Terminated - Stroke Clinical Trials

The Effect Of Acadesine On Reducing Cardiovascular and Cerebrovascular Adverse Events In Coronary Artery Bypass Graft (CABG) Surgery (Study P05633 AM1)(TERMINATED)

RED-CABG
Start date: April 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether acadesine is effective in reducing the cardiovascular and cerebrovascular adverse events in high-risk participants undergoing CABG surgery.