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Clinical Trials/ACTRN12605000677606
ACTRN12605000677606
Not yet recruiting
Phase 4

A randomised phase IV study to compare the effects of propofol and sevoflurane in preventing myocardial necrosis in non-insulin dependent diabetes mellitus patients undergoing coronary artery bypass graft surgery requiring cardiopulmonary bypass.

Dept of Anaesthesia0 sites40 target enrollmentOctober 21, 2005
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ConditionsPostoperative myocardial damageMetabolic and Endocrine - DiabetesCardiovascular -

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Postoperative myocardial damage
Sponsor
Dept of Anaesthesia
Enrollment
40
Status
Not yet recruiting
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 21, 2005
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Dept of Anaesthesia

Eligibility Criteria

Inclusion Criteria

  • •Non insulin dependent diabetes mellitus patients, undergoing routine, primary coronary artery bypass graft surgery requiring cardiopulmonary bypass.

Exclusion Criteria

  • •Those with a sensitivity to propofol or its components, acute or evolving myocardial infarction, peroperative haemodynamic instability, hepatorenal dysfunction, off pump or valvular surgery.

Outcomes

Primary Outcomes

Not specified

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