Clinical Trials Logo
  1. Home
  2. Coronary Occlusion
  3. NCT05848232

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 January 2024
Completion date July 2024
View Details
See also
  Status Clinical Trial Phase
Completed NCT01721096 - XIENCE PRIME Japan Post-Marketing Surveillance (PMS)
Completed NCT00987610 - Guidewire for Chronic Total Occlusion Phase 4
Completed NCT02533128 - Biomarkers, Blood Pressure, BIS: Risk Stratification/Management of Patients at Cardiac Risk in Major Noncardiac Surgery N/A
Completed NCT04246125 - Patient Skin Dose in Interventional Radiology
Completed NCT03717675 - Supplemental Study to Evaluate the Safety and Effectiveness of the NovaCross™ Micro-catheter N/A
Recruiting NCT03588481 - IRIS- DESyne X2 in the IRIS-DES Registry
Recruiting NCT05089864 - STAR and Deferred Stenting Study N/A
Not yet recruiting NCT03719014 - Cohort B of the Pivotal Study to Evaluate the Safety and Effectiveness of the NovaCross™ Micro-catheter N/A
Not yet recruiting NCT02963584 - Decision Aid in Chronic Total Occlusion (CTO) Patients N/A
Completed NCT00793221 - Non-acute Coronary occlusIon Treated By Everolimus ELuting Stent Phase 3
Completed NCT04281212 - Observational Study Evaluating the Management of Chronic Coronary Occlusions In France
Not yet recruiting NCT04562142 - A Novel Non-Invasive Acoustic Diagnostic for the Diagnosis of Coronary Artery Disease The CAD-det Validation Study N/A
Enrolling by invitation NCT02931331 - Coronary Revascularization Assessed by Stress PET N/A
Terminated NCT02683356 - Optical Coherence Tomography to Improve Outcome for Coronary Revascularisation Using Bioresorbable Vascular Scaffolds N/A
Completed NCT00657436 - Myeloid-Related Protein in Evaluation of Acute Chest Pain in the Emergency Departement N/A
Terminated NCT03993522 - Exercise in Patients With a Total Coronary Occlusion N/A
Not yet recruiting NCT03159650 - Comparative Study Between Intravascular Ultrasonography Guided and Angiography-guided Recanalization of Coronary Chronic Total Occlusions N/A
Recruiting NCT02325869 - Clinical Study Protocol - Debris Interventional Removal in ACS (DESIRE-ACS) N/A
Completed NCT00640068 - Advanced Cardiovascular Imaging Consortium N/A
Completed NCT01759290 - ABSORB FIRST is a Registry Designed to Evaluate the Safety and Performance of Absorb Bioresorbable Vascular Scaffold (Absorb BVS) Used in Real-world Patients. N/A