ST Segment Elevation Myocardial Infarction Clinical Trial
— STresolutionOfficial title:
SsST Segment Resolution After Primary Percutaneous Coronary Intervention. A Comparison Between Primary Percutaneous Coronary Intervention With and Without Thrombus Aspiration
Verified date | March 2019 |
Source | Assiut University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
To compare the ST segment resolution after primary percutaneous coronary intervention (PPCI) with and without thrombus aspiration in patients with ST segment elevation myocardial infarction as ST segment resolution is the best indicator for the prediction of the outcome and MACE
Status | Not yet recruiting |
Enrollment | 270 |
Est. completion date | September 1, 2021 |
Est. primary completion date | September 1, 2020 |
Accepts healthy volunteers | |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: . patients with STEMI within 24 hours of chest pain.patients killip class 1 is included in this study xclusion Criteria: - killip II-IV - Previous myocardial infarction - Patients with left bundle branch block - Patients with advanced cancer disease - Patients qith contraindications to anti-coagulation - Patients with sensitivity to clopidogrel |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Assiut University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | ST segment resolution | ST segment resolution in relation to the procedure used in primary percutaneous coronary intervention | Within 90 minutes after the procedure | |
Secondary | MACE | the major adverse coronary events in correlation to ST segment resolution after primary percutaneous coronary intervention (recurrent angina, reinfarction, heart failure, major bleeding, disabling stroke or death) during the period of hospitalization. | one week |
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