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Clinical Trials/NCT00569816
NCT00569816
Completed
Phase 4

A Comparison Between Continuous and Repetitive Sevoflurane Administration for Preconditioning During Coronary Artery Bypass Surgery

University Hospital Schleswig-Holstein1 site in 1 country50 target enrollmentJanuary 2005
InterventionsSevoflurane

Overview

Phase
Phase 4
Intervention
Sevoflurane
Conditions
Myocardial Injury
Sponsor
University Hospital Schleswig-Holstein
Enrollment
50
Locations
1
Primary Endpoint
Myocardial cell damage as assessed by plasma levels of Troponin T
Status
Completed
Last Updated
18 years ago

Overview

Brief Summary

Pharmacologic preconditioning by volatile anesthetics may depend on the mode of administration. The researchers hypothesize that a continuous administration in patients scheduled for CABG surgery prebypass will be less effective in terms of attenuating myocardial cell damage compared to a repetitive administration with a double wash in/wash out schedule. A control group will receive propofol as their primary anesthetic.

Registry
clinicaltrials.gov
Start Date
January 2005
End Date
May 2007
Last Updated
18 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Hospital Schleswig-Holstein

Eligibility Criteria

Inclusion Criteria

  • Patients schedulded to undergo CABG surgery
  • Age 18 to 80 years
  • Ejection fraction \> 40%

Exclusion Criteria

  • Emergency cases
  • Not able to give informed consent
  • Ejection fraction \< 40%

Arms & Interventions

Group 1

Propofol as the primary anesthetic

Intervention: Sevoflurane

Group 2

Sevoflurane administered continuously after induction of anesthesia until initiation of cardiopulmonary bypass.

Intervention: Sevoflurane

Group 3

Sevoflurane administered repetitive up to 1 MAC from induction of anesthesia until initiation of cardiopulmonary bypass. Wash in and wash out performed twice.

Intervention: Sevoflurane

Outcomes

Primary Outcomes

Myocardial cell damage as assessed by plasma levels of Troponin T

Time Frame: from induction of anesthesia until hospital discharge

Secondary Outcomes

  • Length of stay on the ICU and in the hospital(from hospital admission until hospital discharge)

Study Sites (1)

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