NCT05848232View on ClinicalTrials.gov

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

PHASE3Not yet recruitingINTERVENTIONAL
Enrollment

150

Participants

Timeline

Start Date

June 30, 2024

Primary Completion Date

January 31, 2025

Study Completion Date

February 28, 2025

Conditions
Coronary Occlusion
Interventions
DEVICE

coraFlex Catheter

The coraFlex catheter is intended to facilitate the intraluminal placement of conventional guidewires beyond occluded coronary lesions.

DEVICE

coraForce Catheter

The coraForce catheter is intended to facilitate the intraluminal placement of conventional guidewires beyond occluded coronary lesions.

DEVICE

coraCross Catheter

The coraCross catheter is intended to facilitate the intraluminal placement of conventional guidewires beyond occluded coronary lesions.

Trial Locations (1)

98195

University of Washington Medical Center, Seattle

All Listed Sponsors
lead

ReFlow Medical, Inc.

INDUSTRY

NCT05848232 - Single-Arm Study Evaluating Use of the CORA Catheters for the Crossing of Coronary Chronic Total Occlusions | Biotech Hunter | Biotech Hunter