Cardiopulmonary Bypass (CPB) Pumps and Blood Activation

This study is currently recruiting participants.

Verified by University Hospital, Angers, September 2005

Sponsored by:	University Hospital, Angers
Information provided by:	University Hospital, Angers
ClinicalTrials.gov Identifier:	NCT00187967

Purpose

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

MedlinePlus related topics: Coronary Artery Disease

U.S. FDA Resources

Study Type:	Interventional
Study Design:	Treatment, Randomized, Single Blind, Active Control, Parallel Assignment
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

Eligibility

Ages Eligible for Study:	18 Years and older
Genders 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

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: 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

More Information

Study ID Numbers:	PHRC 03-03
Study First Received:	September 9, 2005
Last Updated:	September 24, 2007
ClinicalTrials.gov Identifier:	NCT00187967
Health Authority:	France: Ministry of Health

Study placed in the following topic categories:

Arterial Occlusive Diseases
Coronary Disease
Heart Diseases
Myocardial Ischemia

Vascular Diseases
Arteriosclerosis
Ischemia
Coronary Artery Disease

Additional relevant MeSH terms:

Cardiovascular Diseases

ClinicalTrials.gov processed this record on January 15, 2009