Effects of Nicorandil on Cardiac Infarct Size in Patients With ST-segment

Status Recruiting

Clinical Trial Summary

The purpose of this study is to determine whether nicorandil reduce cardiac infarct size in patient with ST-segment elevation acute myocardial infarction.

Clinical Trial Description

Study objective :

To investiage whether nicorandil treatment reduce infarct size measured by cardiac MRI at 6 months after primary PCI

Allocation :

1. Nicorandil arm :

Recieve nicorandil 4 mg i.v. before undergoing PCI, additionall 2mg i.c. just before 1st ballooning, additionall 2mg i.c. just before stenting, After successful PCI, 10 mg/day (or 5 mg/day) p.o. for 6 months.

2. Control arm :

Recieve standard treatment including PCI, but avoid nicoranil and adenosine.

Follow-up and Measurement :

Cardiac MRI scans are scheduled at 5 days and 6 months after primary PCI. Clinically followed upto 6 months after parimary PCI. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02449070
Study type	Interventional
Source	Pusan National University Hospital
Contact	Jun-Hyok Oh, MD
Phone	82-51-240-7794
Email	jhoh724@hanmail.net
Status	Recruiting
Phase	Phase 3
Start date	May 2015
Completion date	October 2018

View Details

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Effects of Nicorandil on Cardiac Infarct Size in Patients With ST-segment Elevation Acute Myocardial Infarction

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms