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Single-Arm Study Evaluating Use of the CORA Catheters for the Crossing of Coronary Chronic Total Occlusions — Cora CTO  

Coronary Occlusion Clinical Trial

Official title:
A Prospective Single-Arm Multicenter Study Evaluating Use of the CORA Catheters for the Crossing of Coronary Chronic Total Occlusions

Clinical Trial Summary

The goal of this clinical trial is to evaluate the safety and effectiveness of the coraFlex, coraForce, and coraCross catheters for crossing chronic total occlusions of the coronary arteries. The study will compare the rate of procedure success to success rates from previous trials. Participants will undergo percutaneous coronary intervention (PCI) for a chronic total occlusion and be followed for 30 days post-procedure.

Clinical Trial Description

The primary objective of this prospective, multicenter, single arm clinical study is to compare the rate of procedure success of the coraCross, coraForce, and coraFlex catheters in facilitating guidewire placement beyond coronary chronic total occlusions to a pre-defined performance goal based on literature. The study population will consist of those 18 years or older with symptomatic ischemic heart disease, undergoing clinically indicated percutaneous recanalization of an occlusive coronary lesion, and meeting all other eligibility criteria. Measures will be assessed through 30 days post-intervention. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05848232
Study type Interventional
Source ReFlow Medical, Inc.
Contact Sara Finton
Phone 616-633-9178
Email sfinton@reflowmedical.com
Status Not yet recruiting
Phase Phase 3
Start date June 2024
Completion date February 2025
View Details
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