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Clinical Trials/ISRCTN64082539
ISRCTN64082539
Completed
Not Applicable

Antiplatelet Regimen Tailoring after primary Percutaneous Coronary Intervention (ART-PCI): a single centre longitudinal cohort prospective trial

Clinical Centre of Serbia (Serbia)0 sites1,700 target enrollmentFebruary 18, 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
ST-elevation myocardial infarction (STEMI)
Sponsor
Clinical Centre of Serbia (Serbia)
Enrollment
1700
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 18, 2010
End Date
TBD
Last Updated
11 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Clinical Centre of Serbia (Serbia)

Eligibility Criteria

Inclusion Criteria

  • 1\. ST\-elevation myocardial infection (STEMI) patients undergoing primary PCI in our institution
  • 2\. Both genders, aged greater than 18 years
  • 3\. Platelet residual aggregation (PRA) assessed 24 hours after the loading with clopidogrel 600 mg
  • 4\. Control group: 1000 patients enrolled in the RISK\-PCI trial (see http://www.controlled\-trials.com/ISRCTN83474650\) in our centre from February 1st, 2006 till June 1st, 2008, who did not have platelet function assays
  • Low responders to clopidogrel will be subjected to ART if there is no exclusion criteria for ART.

Exclusion Criteria

  • 1\. Not alive until 24 hours from clopidogrel loading 600 mg
  • 2\. Aged greater than 75 years
  • 3\. Percutaneous balloon angioplasty (POBA) without stenting
  • 4\. Failed pPCI
  • 5\. Active bleeding in hospital
  • 6\. Coronary dissection with pericardial collection
  • 7\. Haemoglobin (Hb) less than 80 g/dL needing transfusion in hospital
  • 8\. Simultaneous treatment with oral anticoagulants
  • 9\. Candidates for urgent bypass surgery
  • 10\. Low basal thrombin receptor activating peptide (TRAP) value (less than 500 AU/minute)

Outcomes

Primary Outcomes

Not specified

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