RecruitingNot ApplicableNCT06966674
No-Reflow in Patients With STEMI After Intracoronary Tirofiban After Opening of the Track
Assessment of No-Reflow in Patients With STEMI After Intracoronary Tirofiban After Opening of the Track
Sponsor
Kafrelsheikh University
Enrollment
60 participants
Start Date
May 12, 2025
Study Type
INTERVENTIONAL
Conditions
Summary
This study aims to assess the no-reflow in patients with STEMI after intracoronary glycoprotein IIb/IIIa inhibitors after opening of track in thrombus.
Eligibility
Min Age: 18 Years
Inclusion Criteria3
- Age ≥ 18 years old.
- Both sexes.
- Patients with STEMI. ST-segment elevated myocardial infarction is defined as typical chest pain \>30 minutes with ST-segment elevation of \>1 mm in at least 2 consecutive leads on the electrocardiogram or new-onset left bundle brunch block.
Exclusion Criteria7
- Treatment with thrombolytic drugs in the previous 24 hours.
- Known malignancy.
- Thrombocytopenia.
- End-stage liver disease.
- Cardiogenic shock.
- Renal failure with glomerular filtration\<30 ml/min.
- Contraindication for the use of tirofiban.
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Interventions
DRUGIntracoronary tirofiban
Patients will receive intracoronary tirofiban (Aggrastat®) (25 mg/kg).
DRUGSaline 0.9%
Patients will receive intracoronary saline 0.9% solution as a control group.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06966674
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