Clinical Trials Logo

Coronary Artery Bypass Graft clinical trials

View clinical trials related to Coronary Artery Bypass Graft.

Filter by:

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: NCT01629030 Recruiting - Clinical trials for Coronary Artery Bypass Graft

Risk Factors of Sternal Wound Infection After Coronary Artery Bypass Graft

Start date: June 2012
Phase: N/A
Study type: Observational

The investigators are trying to evaluate the performance of neutrophil and lymphocyte counts as a risk factor of deep sternal wound infection after coronary artery bypass graft surgery.

NCT ID: NCT01596738 Completed - Clinical trials for Coronary Artery Disease

Tranexamic Acid in On-pump CABG With Premature Clopidogrel Cessation

Start date: October 2008
Phase: N/A
Study type: Interventional

The use of platelet aggregation inhibitors, including aspirin and clopidogrel, has become a standard management strategy for patients with acute coronary syndrome. On this background, an increasing percentage of patients presenting for surgical coronary revascularization is the subject to irreversible platelet inhibition. Tranexamic acid is a widely used antifibrinolytic agent, and is a promising substitute for aprotinin when the latter has been suspended in 2007.The release of plasmin during CPB activates fibrinolysis and may contribute to platelet dysfunction. Pharmacological inhibition of the fibrinolytic system may therefore ameliorate platelet dysfunction and fibrinolysis after CPB and decrease postoperative bleeding. Tranexamic acid prevents plasmin formation and inhibits fibrinolysis. Many studies and meta-analyses have shown a reduction in postoperative bleeding and transfusion requirements of this antifibrinolytic drug in cardium revascularization surgery. Unfortunately the preoperative antiplatelet therapy was either neglected or obscure. Few studies specify the time between the last clopidogrel ingestion and surgery.Several studies were keen on the blood loss and allogeneic transfusion in patients who received their last clopidogrel or asprin within 7 days prior to coronary artery bypass grafting. Concerning the secession of aprotinin and the increasing proportion of patients with persistence on clopidogrel until their surgery, evolutional work is expected, especially in the eastern population. The purpose of this study is to assess the effect of tranexamic acid in patients with clopidogrel and asprin ingestion less than 7 days prior to surgery. The working hypothesis is that tranexamic acid would reduce bleeding and transfusion requirements in this specific population of patients.

NCT ID: NCT01591642 Completed - Clinical trials for Coronary Artery Bypass Graft

Physical Activity, Functional Fitness and Quality of Life After Coronary Artery Bypass Grafting

Start date: January 2011
Phase: N/A
Study type: Observational

The main purposes of this study are: (1) to investigate the difference of the physical fitness, and quality of life (QOL) among different physical activity levels in post-coronary artery bypass graft (CABG) patients; (2) to analyze the relationships between physical activity and physical fitness and QOL in this population. The investigators predict physical activity and physical fitness remain limited in patients after CABG, and patients with higher physical activity levels will have higher QOL and physical fitness.

NCT ID: NCT01572454 Completed - Dexmedetomidine Clinical Trials

Comparison of Dexmedetomidine and Remifentanil Infusion During CABG

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

We are trying to investigate whether intraoperative dexmedetomidine infusion could decrease the incidence of intraoperative hypokalemia and arrhythmia, and myocardial injury in patients undergoing off-pump coronary artery bypass graft, and trying compare these effects with those of remifentanil infusion.

NCT ID: NCT01535222 Completed - Clinical trials for Cardiopulmonary Bypass

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of MDCO-2010 in Patients Undergoing Elective Coronary Artery Bypass Graft Surgery

Start date: November 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to demonstrate that periprocedural infusion of escalating doses of MDCO-2010 is safe and tolerated in patients undergoing elective CABG surgery, to characterize the single dose pharmacokinetics of MDCO-2010, to investigate the effect of MDCO-2010 on pharmacodynamics (biomarkers of fibrinolysis and coagulation parameters), and to investigate the effect on exploratory clinical endpoints of bleeding, transfusion requirements and reexploration.

NCT ID: NCT00965471 Completed - Clinical trials for Acute Coronary Syndrome

Effect of Chinese Traditional Medicine for Post Revascularization Treatment of Coronary Artery Disease

Start date: October 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to built the standard of Chinese Traditional Medicine test for Post percutaneous coronary artery intervention and coronary artery bypass graft,also for acute coronary syndrome,according to the multi-site、random large sample test.

NCT ID: NCT00863044 Completed - Clinical trials for Coronary Artery Bypass Graft

High Frequency Ventilation During Off Pump Coronary Artery Bypass Graft (CABG)

VHF
Start date: November 2009
Phase: Phase 4
Study type: Interventional

This study is to test the safety of high frequency-low volume ventilation during off pump coronary artery bypass as reflected in the near infrared spectroscopy values for cerebral oxygenation.

NCT ID: NCT00824759 Withdrawn - Healthy Clinical Trials

Cardioprotective Effects of Increased Endogenous Erythropoietin After Normobaric Oxygen Breathing

Start date: n/a
Phase: N/A
Study type: Interventional

Tissue hypoxia is the only accepted trigger for erythropoietin (EPO) production. However, in healthy subjects EPO concentrations have also increased after oxygen breathing. The aim of our study is to confirm these observations. Besides its main function in erythropoiesis, EPO has also shown tissue protective effects. The second goal of our study is to observe the cardioprotective effects of increased endogenous EPO, induced after normobaric oxygen breathing.

NCT ID: NCT00622791 Completed - Clinical trials for Coronary Artery Disease

Propofol Pharmacokinetics and Pharmacodynamics During Cardiopulmonary Bypass

Start date: n/a
Phase: N/A
Study type: Observational

Cardiopulmonary bypass (CPB) is known to alter pharmacokinetics (PK) and brain sensitivity to several drugs, including propofol. Few studies, however, have tested if propofol pharmacokinetical alterations observed after CPB could contribute to the increased hypnotic effect of propofol after CPB. This study was designed to test the hypothesis that changes in the PK of propofol contribute to an increase in its hypnotic effects after CPB as evidenced by changes in bispectral index (BIS) values. Twenty undergoing coronary artery bypass graft patients will be allocated in two groups: 1) CPB groups and 2) off-pump coronary artery bypass graft. Bispectral Index values and blood samples for plasma propofol concentration measurements will be collected along the surgery and up to 12 hours in the post-operative period. Plasma propofol concentrations, Bispectral index values and propofol PK will be compared between the groups.