Perioperative ischaemic evaluation trial
Phase 3
Completed
- Conditions
- Surgery - Other surgeryPerioperative cardiac morbidity and mortality within 30 days of surgery
- Registration Number
- ACTRN12605000308695
- Lead Sponsor
- MediClin Pty Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 10000
Inclusion Criteria
With or at risk of ischaemic heart disease. Having moderatie or high risk non-cardiac surgery.
Exclusion Criteria
Bradycardia or heart block, bronchospasm, recent CABG surgery, beta-blockers or verapamil.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Perioperative cardiac morbidity[30 days after surgery];Perioperative cardiac mortality[30 days after surgery]
- Secondary Outcome Measures
Name Time Method Safety outcomes[Within 30 days of surgery.]