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Coronary Artery Bypass Grafting clinical trials

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NCT ID: NCT00287209 Completed - Atrial Fibrillation Clinical Trials

Reduction of Atrial Fibrillation Study in Patients Undergoing Coronary Artery Bypass Grafting. (RASCABG 1 Study)

Start date: January 2004
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether postoperatively oral treatment with high dosis amiodarone for five days after intravenously admitted bolusinfusion will minimize the risk for development of atrial fibrillation after coronary artery bypass grafting.

NCT ID: NCT00246740 Completed - Clinical trials for Cardiopulmonary Bypass

Protection of the Heart With Doxycycline During Coronary Artery Bypass Grafting

Start date: October 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether doxycycline (Periostat) at a sub-antimicrobial dose will decrease reperfusion injury after coronary artery bypass grafting (CABG) surgery with cardiopulmonary bypass (CPB).

NCT ID: NCT00226265 Completed - Heart Diseases Clinical Trials

The Short Form-36: Pre- Versus Post-Surgical Administration in Cardiac Surgery Patients

Start date: January 1999
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether the SF-36 can be administered reliably to cardiac surgery patients (two to three days) post-surgery, with the patient answering the questions of this survey from a pre-surgical perspective.

NCT ID: NCT00188006 Completed - Clinical trials for Coronary Artery Bypass Grafting

Complement Activation and Central Nervous System Injury After Coronary Artery Surgery

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

The impact of the postoperative inflammatory response on the central nervous system after cardiac surgery is uncertain. The goal of this study was to evaluate the role of complement activation on cellular brain injury and neurological functioning in patients undergoing coronary artery surgery. In addition, the effect of complement activation on the cerebral vasomotricity was assessed. Because receptors to activated complement are present on astrocytes, the heparin-coated cardiopulmonary bypass that reduces complement activation should minimize these postoperative neurological adverse events. Heparin-coating might also influence blood flow velocity in cerebral arteries postoperatively if complement activation mediates cardiopulmonary bypass induced cerebral vasomotor dysfunction.

NCT ID: NCT00169832 Completed - Diabetes Clinical Trials

Vein-Coronary Atherosclerosis And Rosiglitazone After Bypass Surgery: The VICTORY Trial

VICTORY
Start date: June 2003
Phase: Phase 3
Study type: Interventional

HYPOTHESES - Rosiglitazone in diabetic patients with previous coronary bypass surgery may prevent or slow the progression of atherosclerosis in SVGs and native coronary arteries. - Rosiglitazone has favorable effects on adipose tissue distribution variables as well as on thrombosis, pro-inflammatory, and lipid profiles in diabetic patients after coronary bypass artery surgery. - Rosiglitazone therapy influences favorably metabolism and clinical outcomes in diabetic patients after coronary artery bypass surgery. OBJECTIVES - PRIMARY To assess the efficacy of rosiglitazone to reduce atherosclerosis progression in vein grafts in diabetic patients after coronary bypass surgery by using IVUS imaging after a 12 mo follow-up. - SECONDARY - To prospectively compare the secondary IVUS endpoints. - To prospectively compare the angiographic endpoints. - To prospectively compare the metabolic risk factor endpoints. - To prospectively compare the body composition and distribution endpoints. - To prospectively compare the clinical outcomes of rosiglitazone versus standard care using composite endpoints.