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Cardiopulmonary Bypass (CPB) Pumps and Blood Activation

NCT00187967 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2007-09-26

No results posted yet for this study

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.

Conditions

Interventions

DEVICE

pumps used for cardiopulmonary bypass

Sponsors & Collaborators

  • University Hospital, Angers

    lead OTHER_GOV

Principal Investigators

  • Christophe Baufreton, MD, PhD · University Hospital of Angers, France

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-01-31

Countries

  • France

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00187967 on ClinicalTrials.gov