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Cardioprotection for type II diabetic patients undergoing cardiopulmonary bypass: a comparison of 2 different anaesthetic agents.

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.

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12605000677606
Acronym
N/A
Enrollment
40
Registered
2005-10-21
Start date
2006-01-01
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Diabetic patients will be randomised to receive one of two commonly used anaesthetic drugs to maintain general anaesthesia whilst on cardiopulmonary bypass. We will be investigating which one offers better cardioprotection as determined by measuring an enzyme called cardiac troponin i. This enzyme is commonly measured to detect whther a myocardial infarction "heart attack" has occurred.

Interventions

A comparison of 2 different anaesthetic agents (propofol and sevoflurane) and their affect on cardioprotection in non insulin diabetic patients undergoing coronary artery bypass graft surgery requiring cardiopulmonary bypass. 2 groups of 20 patients each will be randomised to receive either propofol or sevoflurane to maintain general anaesthesia whilst on cardiopulmonary bypass. Anaesthesia leading up to bypass will be the same in each group. At 15 minutes post separation from bypass, both gr

A comparison of 2 different anaesthetic agents (propofol and sevoflurane) and their affect on cardioprotection in non insulin diabetic patients undergoing coronary artery bypass graft surgery requiring cardiopulmonary bypass. 2 groups of 20 patients each will be randomised to receive either propofol or sevoflurane to maintain general anaesthesia whilst on cardiopulmonary bypass. Anaesthesia leading up to bypass will be the same in each group. At 15 minutes post separation from bypass, both groups will receive sevoflurane anaesthesia alone. Otherwise, management will be as per normal for coronary artery bypass patients.

Sponsors

Dept of Anaesthesia
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Other
Primary purpose
Prevention
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
0 to 80 Years
Healthy volunteers
No

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.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026