Cardiopulmonary Bypass (CPB) Pumps and Blood Activation

Blood Activation During Cardiopulmonary Bypass Using Roller or Centrifugal Pumps

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00187967

Enrollment

Unknown

Registered

2005-09-16

Start date

2005-01-31

Completion date

Unknown

Last updated

2007-09-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiopulmonary Bypass, Coronary Artery Disease

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.

Interventions

DEVICEpumps used for cardiopulmonary bypass

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

SINGLE

Eligibility

Sex/Gender

MALE

Age

18 Years to No maximum

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

Countries

France

Contacts

Primary ContactAnthony Bailleul

33-(0)2-41-35-58-91

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026