ACTRN12610000876099
Terminated
未知
A Randomised Controlled Trial in Adult Patients Undergoing Coronary Artery Bypass Graft Surgery Designed to Determine the Optimal Dose for Remote Ischaemic Preconditioning Compared to No Remote Ischaemic Preconditioning and Measuring the Primary Outcome of Area Under the Curve for Troponin to 72 hours Post Aortic Cross Clamp Removal.
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Coronary Artery Bypass Graft Surgery
- Sponsor
- Medical Research Institute of New Zealand
- Enrollment
- 96
- Status
- Terminated
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Undergoing coronary artery bypass graft surgery with cardiopulmonary bypass
Exclusion Criteria
- •1\. documented ejection fraction \<50%,
- •2\. concurrent valvular surgery,
- •3\. myocardial infarction within 21 days,
- •4\. possible radial artery harvesting,
- •5\. planned cross\-clamp fibrillation,
- •6\. \>85 years of age,
- •7\. peripheral vascular disease affecting the upper limbs
- •8\. taking the sulphonylurea glibenclamide
Outcomes
Primary Outcomes
Not specified
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