Patients with acute heart attack. ST elevation (STEMI) and non-ST elevation (NSTEMI) myocardial infarction
Conditions
Interventions
Intervention 1: Intervention group: 2 mg of oral colchicine as a loading dose (two tablets) then 0.5 mg (half a tablet) of colchicine twice a day (every 12 hours) for 30 days. Intervention 2: Control
Sponsors
Oroumia University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: Patients who have ST elevation myocardial infarction and are candidates for primary percutaneous intervention
Exclusion criteria
Exclusion criteria: Hemodynamic instability liver failure kidney failure history of blood disease chronic colchicine use
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Investigation of TIMI flow rate in coronary arteries after stent placement in acute myocardial infarction patients. Timepoint: After the intervention and at the beginning of the study. Method of measurement: Judgment by cardiologist after angiography. | — |
Secondary
| Measure | Time frame |
|---|---|
| Examination of the small amount of TROPONIN. Timepoint: at admission and 24 and 48 hours later. Method of measurement: in the laboratory by quantitative troponin kits.;Investigating the increase of CRP. Timepoint: at the beginning of hospitalization and 48 hours later. Method of measurement: Measurement by quantitative kits in the laboratory. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactOzra Kahourian
Oroumia University of Medical Sciences
Outcome results
None listed