Clinical Trial

Remote Ischemic Conditioning Using the autoRIC

Study Description

Remote Ischemic Conditioning Using the autoRIC

The purpose of the study is to evaluate the hypothesis that patients receiving remote ischemic conditioning using the autoRIC device show statistically significant reduction in the prevalence of ischemia-reperfusion injury to the myocardium as compared to patients in the autoRIC Sham device arm (within 12-24 hours post non-emergent PCI with stent implantation).

Location

Locations Selected Location

Methods

No pharmaceutical medication involved No pharmaceutical medication involved
Recruiting patients only Recruiting patients only

Device - autoRIC

Automated Remote Ischemic Conditioning

Device - autoRIC Sham

Automated Remote Ischemic Conditioning Sham

Additional Information

Official Study Title

Safety and Effectiveness of Remote Ischemic Conditioning With the autoRIC Prior to Elective Percutaneous Coronary Intervention (PCI) Study

Clinical Trial ID

NCT03318575

ParticipAid ID

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