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Cardiac Surgery clinical trials

View clinical trials related to Cardiac Surgery.

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NCT ID: NCT00547859 Completed - Cardiac Surgery Clinical Trials

Relationship Between Microcirculatory Flow Alterations and Tissue Metabolism

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

The purpose of this study is to correlate microcirculatory flow and rectal anaerobe cellular CO2 production in patients after cardiac surgery. The hypothesis is that such a correlation exists.

NCT ID: NCT00545506 Terminated - Cardiac Surgery Clinical Trials

The Influence of a Warmed Surgical Bandage System on Subcutaneous Tissue Oxygen Tension After Cardiac Surgery

Start date: November 2007
Phase: Phase 3
Study type: Interventional

Warmed Surgical Bandage may improve tissue oxygenation and thus on the long run reduce wound infections

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: NCT00515736 Terminated - Trauma Clinical Trials

Impact Of Antioxidant Micronutrients On Intensive Care Unit (ICU) Outcome

Etude-AOX
Start date: January 2003
Phase: Phase 3
Study type: Interventional

Critically ill patients are generally exposed to an increased oxidative stress, which is proportional to the severity of their condition. Endogenous antioxidant (AOX) defenses are depleted particularly in those patients with intense inflammatory response. The hypothesis tested is that early I:V: administration of a combination of AOX micronutrient supplements (Se, Zn, Vit C, Vit E, Vit B1) would improve clinical outcome in selected critically ill patients, by reinforcing the endogenous AOX defenses and reducing organ failure.

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: NCT00426894 Not yet recruiting - Cardiac Surgery Clinical Trials

Microbial Surveillance in Children Hospitalized for Cardiovascular Surgery

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

the purpose of this study is to determine whether children who are hospitalised waiting for cardiac surgery for several days in pediatric or pediatric surgery department acquire resistant microbial flora, thus necessitating broad spectrum antibiotics for perioperative prophylaxis.

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.