Mean Platelet Volume and STEMI Clinical Risk Scores in Prediction of Impaired Myocardial Perfusion In Acute STEMI Patients Undergoing Primary Percutaneous Coronary Intervention.

Completed

• Conditions: No-Reflow Phenomenon

• Registration Number: NCT04785209
• Lead Sponsor: Assiut University

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study Start: 2020-09-01
• Study First Submitted: 2020-09-23
• Primary Completion: 2021-02-28
• Study First Submitted QC: 2021-03-02
• Study First Posted: 2021-03-05
• Status Verified: 2024-05
• Study Completion: 2024-05-01
• Last Update Submitted: 2024-05-30
• Last Update Posted: 2024-05-31

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 640

Inclusion Criteria

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

Exclusion Criteria

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

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

Trial Locations

Locations (1)

Assiut university hospital; 🇪🇬 Assiut, Egypt