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临床试验/NCT05175261
NCT05175261已完成不适用

Assessment of Individual Risk of Cardiovascular Events by Platelet FcGammaRIIa

Prolocor, Inc1 个研究点 分布在 1 个国家目标入组 764 人开始时间: 2022年1月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Prolocor, Inc
入组人数
764
试验地点
1
主要终点
Ischemic

研究概览

简要总结

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.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

结局指标

主要结局

Ischemic

时间窗: 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

次要结局

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

研究者

发起方
Prolocor, Inc
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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