Randomized Isoflurane and Sevoflurane Comparison in Cardiac Surgery

PHASE4CompletedINTERVENTIONAL
Enrollment

464

Participants

Timeline

Start Date

November 30, 2011

Primary Completion Date

March 31, 2015

Study Completion Date

March 31, 2015

Conditions
Coronary Artery DiseaseValvular Heart Disease
Interventions
DRUG

Volatile anesthetic

"The intervention in this trial is randomization to either maintenance of anesthesia with sevoflurane or maintenance of anesthesia with isoflurane. The designated volatile anesthetic will be given at a strict minimal amount throughout the entire cardiac surgery (including cardiopulmonary bypass). This regimen (administration throughout the entire operation) has proved to have the greatest efficacy. Apart from this intervention, the anesthetic for patients participating in this trial will not be substantially different from normal practice, as the intention is to allow normal practice (with the exception of the choice of volatile anesthetic agent) to maximize the applicability and external validity of the trial. The management of anticoagulation, cardiac surgical techniques, and other aspects of the procedure will be managed in an unaltered fashion.~No IV drug infusions will be permitted until after protamine administration."

Trial Locations (1)

N6A5A5

University Hospital - London Health Sciences Centre, London

All Listed Sponsors
lead

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

OTHER

NCT01477151 - Randomized Isoflurane and Sevoflurane Comparison in Cardiac Surgery | Biotech Hunter | Biotech Hunter