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

No-Reflow Phenomenon Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04785209
• Other study ID #: Prediction of No reflow
• Status: Completed
• Start date: September 1, 2020
• Est. completion date: May 1, 2024

Study information

• Verified date: May 2024
• Source: Assiut University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

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

Recruitment information / eligibility

• Status: Completed
• Enrollment: 640
• Est. completion date: May 1, 2024
• Est. primary completion date: February 28, 2021
• Gender: All
• Age group: 16 Years and older

Eligibility

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

Related Conditions & MeSH terms

• No-Reflow Phenomenon

Intervention

Other:
• Mean platelet volume, lymphocyte number, STEMI clinical risk scores
Lab parameters

Locations

Country	Name	City	State
Egypt	Assiut university hospital	Assiut

Sponsors (1)

Lead Sponsor	Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of participents with No reflow after PPCI and in hospital mortality	No reflow: suboptimal myocardial reperfusion through a part of coronary circulation without angiographic evidence of mechanical vessel obstruction.; In hospital mortality	Within 48 hours from admission