Cardiopulmonary Bypass (CPB) Pumps and Blood Activation

Not Applicable

• Conditions: Cardiopulmonary Bypass; Coronary Artery Disease

• Registration Number: NCT00187967
• Lead Sponsor: University Hospital, Angers

Brief Summary

Blood activation induced by cardiopulmonary bypass may compromise the postoperative outcome. The goal of this study is to compare blood activation induced by cardiopulmonary bypass performed with centrifugal pump or roller pump in patients undergoing coronary artery surgery.

Detailed Description

Not available

Study Timeline

• Study Start: 2005-01
• Status Verified: 2005-09
• Study First Submitted: 2005-09-09
• Study First Submitted QC: 2005-09-09
• Study First Posted: 2005-09-16
• Last Update Submitted: 2007-09-24
• Last Update Posted: 2007-09-26

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: Male
• Target Recruitment: Not specified

Inclusion Criteria

• Men undergoing coronary artery bypass grafting using cardiopulmonary bypass
• Aspirin therapy

Exclusion Criteria

• Redo surgery
• Acute coronary syndrome requiring urgent surgery
• Oral anticoagulant therapy
• Organ dysfunction or chronic inflammatory disease
• Surgery other than coronary artery bypass grafting

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Trial Locations

Locations (1)

University Hospital of Angers; 🇫🇷 Angers, France