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临床试验/NCT04785209
NCT04785209已完成不适用

Mean Platelet Volume and STEMI Clinical Risk Scores in Prediction of Impaired Myocardial Perfusion In Acute STEMI Patients Undergoing PPCI.

Assiut University1 个研究点 分布在 1 个国家目标入组 640 人开始时间: 2020年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
640
试验地点
1
主要终点
Number of participents with No reflow after PPCI and in hospital mortality

研究概览

简要总结

Predicting no reflow in ppci of STEMI patients using mean platelet volume together with STEMI clinical risk scores

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

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

入选标准

  • patients presenting with acute STEMI, within 24 hours of symptoms, fulfilling criteria for PPCI protocol in our facility

排除标准

  • patients presenting more than 24 hours of symptoms onset
  • patients not eligible for PPCI program in our facility

结局指标

主要结局

Number of participents with No reflow after PPCI and in hospital mortality

时间窗: Within 48 hours from admission

No reflow: suboptimal myocardial reperfusion through a part of coronary circulation without angiographic evidence of mechanical vessel obstruction. In hospital mortality

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Andrew Reymon Sadik Salama

Principle invistigator

Assiut University

研究点 (1)

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