Optimal Timing of Coronary Intervention in Unstable Angina 2.

• Conditions: STE-ACS; treatment strategy; Treatment Outcome; Time factorsNon ST hart infarct; Behandel strategie; Behandel uitkomsten; Tijdsfactor

• Registration Number: NL-OMON26173
• Lead Sponsor: Cardiology Research Department, Onze Lieve Vrouwe Gasthuis

Brief Summary

/A

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 350

Inclusion Criteria

1. Age > 21 years;

2. Typical chest pain for angina pectoris lasting at least 10 minutes, within the last 24 hours;

Exclusion Criteria

1. Acute ST myocardial infarction;

2. Refractory angina;

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Size of MI during initial hospitalization as measured by the AUC of CK-MB.

Secondary Outcome Measures

Name	Time	Method
1. Size of MI during initial hospitalization as measured by the AUC of CK-MB for the subpopulation of patients treated with PCI;<br /><br>2. The composite endpoint of death, MI and unplanned revascularization at 30 days;<br /><br>3. The composite endpoint of MI and major haemorrhage;<br /><br>4. Incidence of major haemorrhage up to 30 days;<br /><br>5. Incidence of minor haemorrhage up to 30 days;<br /><br>6. Incidence of individual and composite endpoints at 30 days and 6 and 12 months and 5 years including recurrent NSTE-ACS;<br /><br>7. Any revascularisation and/or restenosis (TVR) up to 6 months;<br /><br>8. Re-hospitalisation because of coronary artery disease (CAD).