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Cardiac Surgery clinical trials

View clinical trials related to Cardiac Surgery.

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NCT ID: NCT00524472 Completed - Cardiac Surgery Clinical Trials

Outcomes Study of Hyperinsulinemic Glucose Control in Cardiac Surgery

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

Patients undergoing cardiac surgery will be randomized into one of two groups. Group A will be administered insulin using the hyperinsulinemic-normoglycemic clamp to normalize blood glucose levels intra-operatively. Group B will be administered insulin at the standard of care levels established by the participating institution. Patients will be followed at 10 days, 15 days and one year post-operatively.

NCT ID: NCT00519337 Completed - Inflammation Clinical Trials

Impact of Ascorbic Acid on Post-Cardiothoracic Surgery Inflammation

AFIST
Start date: October 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to see if ascorbic acid (Vitamin-C) therapy will reduce inflammation following heart surgery.

NCT ID: NCT00470444 Completed - Cardiac Surgery Clinical Trials

Transfusion Triggers in Cardiac Surgery

TTRICS
Start date: December 2006
Phase: N/A
Study type: Interventional

A high proportion of patients having cardiac surgery receive red cell transfusions. Yet, the investigators do not know whether transfusions are beneficial and they may be associated with harm. It is thus important to determine when a transfusion is required. The investigators will conduct a small pilot study at St. Michael's Hospital to address this issue. Patients having cardiac surgery will be allocated to one of two transfusion strategies with endpoints being compliance with the transfusion strategy and clinical outcome. The results of this study will be used to design a large definitive multicentered trial of these two transfusion strategies.

NCT ID: NCT00458783 Completed - Cardiac Surgery Clinical Trials

Red Cell Storage Duration and Outcomes in Cardiac Surgery

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

The purpose of this study is to determine whether length of storage of RBC is related to postoperative morbid outcomes in patients undergoing cardiac surgery.

NCT ID: NCT00451776 Completed - Cardiac Surgery Clinical Trials

Post Operative Hemodynamic Function After Anesthetic Induction With Etomidate for Cardiac Surgery With ECC

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

Because of its hemodynamic safety, etomidate is widely used for anaesthesia induction of cardiac surgery. It can also cause adrenal insufficiency during the following 48 hours ( 11 betahydroxylase inhibition ). So it could increase hemodynamic dysfunction caused by the SIRS following cardiopulmonary bypass. A previous observational study found more adrenal insufficiency and need for vasopressive support therapy in the etomidate group versus another propofol induced group. The aim of our work is to compare hemodynamic dysfunction following induction with etomidate for cardiac surgery with ECC. The control group would be induced by Propofol. 94 patients would be included.

NCT ID: NCT00416299 Completed - Cardiac Surgery Clinical Trials

Prognostic Value of New Cardiac Biomarkers in Elderly Patients Undergoing Cardiac Surgery

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

To evaluate the use of new cardiac biomarker for the prediction of in-hospital cardiovascular complications in elderly patients undergoing elective cardiac surgery.

NCT ID: NCT00338234 Completed - Anemia Clinical Trials

Observational Study of Iron Metabolism in Anemia in ICU and Post-Operative Patients

FAIRe
Start date: June 2006
Phase: N/A
Study type: Observational

Anemia in intensive care and post-operative patients is due to both blood loss (leading to iron loss) and inflammation.

NCT ID: NCT00337805 Completed - Cardiac Surgery Clinical Trials

Double Blind Randomized Trial of Saline vs Pentaspan for Resuscitation After Cardiac Surgery

Start date: September 2004
Phase: Phase 2/Phase 3
Study type: Interventional

This is a randomized double blind trial of the use of the use of colloids vs crystalloid solutions for resuscitation of patients after cardiac surgery. Patients are managed with an algorithm driven protocol that is based on the flow response to fluid challenges. The hypothesis is that the use of a colloid solution will result in less use of catecholamines at 8:00 the morning following surgery. Secondary end-points include total use of catecholamines, time in the ICU, return to the ICU, and safety issues including bleeding and renal function.

NCT ID: NCT00336466 Completed - Cardiac Surgery Clinical Trials

The Erythropoietin NeuroProtective Effect: Assessment in CABG Surgery (TENPEAKS)

Start date: September 2004
Phase: Phase 2
Study type: Interventional

Context: Neurocognitive dysfunction complicates coronary artery bypass graft surgery. Neurocognitive dysfunction is a measurable problem with thinking. Erythropoietin may be a neuroprotectant. Objective: To investigate the feasibility and safety of three doses of human recombinant erythropoietin to reduce neurocognitive dysfunction in coronary artery bypass graft patients.

NCT ID: NCT00334009 Completed - Cardiac Surgery Clinical Trials

Catecholamine-O-Methyl-Transferase(COMT)-Polymorphism in Cardiac Surgery

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

Although clinical risk factors for postoperative development of vasodilatory shock and acute renal failure have been identified; there is a considerable proportion of patients undergoing cardiac surgery where this syndrome cannot be predicted. We sought to investigate the impact of Catecholamine-O-Methyltransferase (COMT) polymorphism on the duration of vasodilatory shock and other important clinical outcomes in cardiac surgery patients. COMT is a key enzyme in the degradation of catechols eg. catecholamines. 25% of the population have a low activity (L/L) of this enzyme. Sustained low COMT activity is associated with an altered metabolic profile of catecholamines and their degradation products. The process of cardiopulmonary bypass (CPB)over-activates some of the same mechanisms the body uses to defend itself against severe infection. One of the main overactive defence mechanisms is the release of highly toxic compounds derived from oxygen - a process called 'oxidative-stress'. Increased reactive oxygen species (ROS) generation can lead to inactivation of biologic mediators, including catecholamines. It is well established that some radicals autoxidizes catecholamines, including DA, NE, and epinephrine and contribute significantly to vasoplegia. As part of this study, we will take six 2.7mL samples of blood, collected before, and after the operation, from the arterial catheter routinely inserted in every patient. This blood will be used to measure COMT genotype, the concentration of plasma-catecholamines as well as marker of oxidative stress. Our plan is to enrol patients undergoing cardiac surgery if the use of the CPB is planned.