TiMing of Intervention in patients with Acute Coronary Syndromes

Not Applicable

Completed

• Conditions: Acute coronary syndromes (unstable angina and non-ST segment elevation myocardial infarction); Circulatory System; Angina pectoris

• Registration Number: ISRCTN20993046
• Lead Sponsor: Population Health Research Institute (PHRI) (Canada)

Brief Summary

2009 results in: https://www.ncbi.nlm.nih.gov/pubmed/19458363 (added 10/04/2019)

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2006-11-27
• Study Completion: 2008-05-01
• Last Update Posted: 5 May 2019

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 4000

Inclusion Criteria

1. Patients presenting or admitted to hospital with symptoms suspected to represent an acute coronary syndrome (unstable angina or MI without persistent ST elevation), i.e. clinical history consistent with new onset, or a worsening pattern, of characteristic ischaemic chest pain or ischaemic symptoms occurring at rest or with minimal activity (lasting longer than five minutes or requiring sublingual nitroglycerin for relief of the pain)
2. Able to randomise within 24 hours of the onset of the most recent episode of symptoms
3. At least two of the three following additional criteria:
3.1. Age more than or equal to 60 years, either sex
3.2. Troponin T or I or creatine kinase - myocardial bands (CK-MB) above the upper limit of normal for the local institution
3.3. Electrocardiogram (ECG) changes compatible with ischaemia (i.e., ST depression at least 1 mm in two contiguous leads or T wave inversion mroe than 3 mm or any dynamic ST shift or transient ST elevation)
4. Written informed consent dated and signed

Exclusion Criteria

1. Age less than 21 years
2. Not a suitable candidate for revascularisation
3. Co-morbid condition with life expectancy less than six months

Study & Design

• Study Type: Interventional
• Study Design: Not specified