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Clinical Trial Summary

A multi-center randomized post-approval evaluation of delivery of intracoronary hyperoxemic supersaturated Oxygen therapy for 60 minutes in anterior AMI patients with successful reperfusion (via PCI) within 6 hours after onset of symptoms compared to standard therapy


Clinical Trial Description

This is a prospective, open-label, randomized (1:1) study. Subjects who present with anterior STEMI requiring stent placement in the proximal and/or mid LAD who meet all inclusion and exclusion criteria and provide informed consent will be treated with PCI with stenting, and if successful and uncomplicated then immediately randomized to post-procedure infusion of SSO2 Therapy for a duration of 60 minutes or standard of care. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04743245
Study type Interventional
Source TherOx
Contact Jeffrey Creech, PhD
Phone 3233096949
Email jcreech@zoll.com
Status Recruiting
Phase N/A
Start date August 2, 2022
Completion date April 30, 2026

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