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

A

Assiut University

Status

Completed

Conditions

No-Reflow Phenomenon

Treatments

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

Study type

Observational

Funder types

Other

Identifiers

NCT04785209
Prediction of No reflow

Details and patient eligibility

About

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

Enrollment

640 patients

Sex

All

Ages

16+ years old

Volunteers

No Healthy Volunteers

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

Trial design

640 participants in 2 patient groups

No complication
Description:
Thrombolysis in myocardial infarction flow grade III flow after PPCI, mean platelet volume, lymphocyte ratio, detailed echo within 24 hrs of admission, clinical STEMI risk scores
Treatment:
Other: Mean platelet volume, lymphocyte number, STEMI clinical risk scores
No reflow
Description:
No reflow phenomenon after pci on STEMI patients, mean platelet volume, lymphocyte ratio, detailed echo within 24 hrs of admission, clinical STEMI risk scores
Treatment:
Other: Mean platelet volume, lymphocyte number, STEMI clinical risk scores

Trial contacts and locations

1

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Central trial contact

Andrew Salama, Resident; Shaimaa Khedr, Assistant lecturer

Data sourced from clinicaltrials.gov

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