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Cardiopulmonary Bypass (CPB) Pumps and Blood Activation

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified September 2005 by University Hospital, Angers.
Recruitment status was:  Recruiting
Information provided by:
University Hospital, Angers Identifier:
First received: September 9, 2005
Last updated: September 24, 2007
Last verified: September 2005
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.

Condition Intervention
Cardiopulmonary Bypass Coronary Artery Disease Device: pumps used for cardiopulmonary bypass

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single
Primary Purpose: Treatment
Official Title: Blood Activation During Cardiopulmonary Bypass Using Roller or Centrifugal Pumps

Further study details as provided by University Hospital, Angers:

Study Start Date: January 2005

Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   Male

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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT00187967

Contact: Anthony Bailleul 33-(0)2-41-35-58-91

University Hospital of Angers Recruiting
Angers, France, 49933
Contact: Christophe Baufreton, MD, PhD    33-(0)2-41-35-45-73   
Contact: Anthony Bailleul    33-(0)2-41-35-58-91      
Sponsors and Collaborators
University Hospital, Angers
Principal Investigator: Christophe Baufreton, MD, PhD University Hospital of Angers, France
  More Information Identifier: NCT00187967     History of Changes
Other Study ID Numbers: PHRC 03-03
Study First Received: September 9, 2005
Last Updated: September 24, 2007

Additional relevant MeSH terms:
Coronary Artery Disease
Myocardial Ischemia
Coronary Disease
Heart Diseases
Cardiovascular Diseases
Arterial Occlusive Diseases
Vascular Diseases processed this record on August 18, 2017