Over-sized stenting in primary percutaneous coronary interventio

Not Applicable

• Conditions: Patient with acute myocardial infarction undergoing primary coronary angioplasty.; ST elevation (STEMI) myocardial infarction of unspecified site; I21.3

• Registration Number: IRCT20190411043242N1
• Lead Sponsor: Rajaie cardiovascular medical and research center

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 October 2019

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 94

Inclusion Criteria

Patients with acute myocardial infarction with >0.1 mV ST-segment elevation from baseline in at least two contiguous leads on the 12-lead electrocardiogram who were candidate for primary percutaneous intervention

Exclusion Criteria

Primary percutaneous coronary intervention without stenting
Primary percutaneous coronary intervention of saphenus vein graft
Rescue Primary percutaneous coronary intervention
stent thrombosis myocardial infarction
Electrocardiogram data inadequate to measure ST resolution

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Cardiac enzyme level. Timepoint: twelve hours after procedure. Method of measurement: Lab kit.;ST segment resolution. Timepoint: 60 minute after procedure. Method of measurement: electrocardiogram.;No Reflow phenomenon. Timepoint: after stent implantation. Method of measurement: angiography.;Hospital stay. Timepoint: hospital course. Method of measurement: patient profile.

Secondary Outcome Measures

Name	Time	Method
Target vessel revascularization. Timepoint: six months after intervention. Method of measurement: Medical record.;Reinfarction. Timepoint: six months after intervention. Method of measurement: Medical record.;Cardiovascular death. Timepoint: six months after intervention. Method of measurement: Medical record.;All cause death. Timepoint: six months after intervention. Method of measurement: Medical record.;Congestive heart failure. Timepoint: six months after intervention. Method of measurement: Medical record.;Cardiovascular accident. Timepoint: six months after intervention. Method of measurement: Medical record.