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Cardiopulmonary Bypass (CPB) Pumps and Blood Activation

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ClinicalTrials.gov Identifier: NCT00187967
Recruitment Status : Unknown
Verified September 2005 by University Hospital, Angers.
Recruitment status was:  Recruiting
First Posted : September 16, 2005
Last Update Posted : September 26, 2007
Sponsor:
Information provided by:
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.

Condition or disease Intervention/treatment
Cardiopulmonary Bypass Coronary Artery Disease Device: pumps used for cardiopulmonary bypass

Study Type : Interventional  (Clinical Trial)
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single
Primary Purpose: Treatment
Official Title: Blood Activation During Cardiopulmonary Bypass Using Roller or Centrifugal Pumps
Study Start Date : January 2005




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

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00187967


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

Locations
France
University Hospital of Angers Recruiting
Angers, France, 49933
Contact: Christophe Baufreton, MD, PhD    33-(0)2-41-35-45-73    ChBaufreton@chu-angers.fr   
Contact: Anthony Bailleul    33-(0)2-41-35-58-91      
Sponsors and Collaborators
University Hospital, Angers
Investigators
Principal Investigator: Christophe Baufreton, MD, PhD University Hospital of Angers, France

ClinicalTrials.gov Identifier: NCT00187967     History of Changes
Other Study ID Numbers: PHRC 03-03
First Posted: September 16, 2005    Key Record Dates
Last Update Posted: September 26, 2007
Last Verified: September 2005

Additional relevant MeSH terms:
Coronary Artery Disease
Myocardial Ischemia
Coronary Disease
Heart Diseases
Cardiovascular Diseases
Arteriosclerosis
Arterial Occlusive Diseases
Vascular Diseases