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Clinical Trials/NCT05175261
NCT05175261
Completed
Not Applicable

Assessment of Individual Risk of Cardiovascular Events by Platelet FcGammaRIIa

Prolocor, Inc1 site in 1 country764 target enrollmentJanuary 20, 2022
ConditionsSTEMINSTEMI

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
STEMI
Sponsor
Prolocor, Inc
Enrollment
764
Locations
1
Primary Endpoint
Ischemic
Status
Completed
Last Updated
7 months ago

Overview

Brief Summary

This is a Prospective, Observational Multicenter Non-Interventional Cohort Study. The primary objective is to determine whether platelet expression of FcγRIIa is associated with risk of myocardial infarction (MI), stroke and death. Secondary objectives include: 1) Develop a score that combines clinical characteristics plus platelet expression of FcγRIIa to determine the risk of MI, stroke, and death; and 2) Determine whether platelet expression of FcγRIIa is associated with risk of major bleeding. The primary endpoint is the composite of death, MI and stroke. A secondary endpoint is the incidence of clinically significant bleeding according to the Bleeding Academic Research Consortium (BARC) scale type 2-5. Approximately 800 male and female subjects with confirmed MI [ST-segment elevation MI (STEMI) or non-ST-segment elevation MI (NSTEMI)] will be enrolled before hospital discharge for the index event. Approximately 10 sites in the United States will participate in this study. It is anticipated that it will take approximately 12 months to enroll approximately 800 subjects. The study and subject follow-up will continue until 1) at least 80 ischemic events (MI, stroke, and death) have occurred, and 2) the last subject enrolled has completed 18 months of follow-up.

Registry
clinicaltrials.gov
Start Date
January 20, 2022
End Date
May 22, 2025
Last Updated
7 months ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Type 1 Myocardial Infarction (STEMI and NSTEMI)
  • Must have ≥ 2 of the following risk factors:
  • Multi-vessel coronary artery disease (MVD) defined as ≥2 vessels or left main with a stenosis ≥50%
  • Chronic kidney disease (CKD) defined as estimated glomerular filtration rate (GFR) ˂ 60 mL/min/1.73 m2
  • Diabetes mellitus (DM)
  • Must agree to participate in the study, to comply with all study procedures and follow-up contact
  • Signed the informed consent form

Exclusion Criteria

  • Requirement for treatment with full dose anticoagulant therapy (e.g., for atrial fibrillation)
  • Participation in another trial in which the subject is known to receive or could receive anticoagulant or antiplatelet treatment as part of the trial intervention.
  • Non-cardiovascular conditions that, in the judgment of the investigator, will limit survival to less than 2 years

Outcomes

Primary Outcomes

Ischemic

Time Frame: Study Duration (up to 3 years)

compare the hazard ratio for first occurrence of myocardial infarction (MI), stroke and death in patients with high vs low platelet FcGammaRIIa

Secondary Outcomes

  • Risk Score(Study Duration (up to 3 years))
  • Bleeding(Study Duration (up to 3 years))

Study Sites (1)

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