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Continuous Versus Repetitive Sevoflurane Administration for Preconditioning

U

University Hospital Schleswig-Holstein (UKSH)

Status and phase

Completed
Phase 4

Conditions

Myocardial Injury

Treatments

Drug: Sevoflurane

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT00569816
UKSHCK-Anae07/06
ACA-GmbH-03-7

Details and patient eligibility

About

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.

Enrollment

50 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 3 patient groups

Group 1
Active Comparator group
Description:
Propofol as the primary anesthetic
Treatment:
Drug: Sevoflurane
Group 2
Experimental group
Description:
Sevoflurane administered continuously after induction of anesthesia until initiation of cardiopulmonary bypass.
Treatment:
Drug: Sevoflurane
Group 3
Experimental group
Description:
Sevoflurane administered repetitive up to 1 MAC from induction of anesthesia until initiation of cardiopulmonary bypass. Wash in and wash out performed twice.
Treatment:
Drug: Sevoflurane

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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