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A Prospective, First in Man Study to Evaluate the Safety and Performance of the NovaCross™ Micro-catheter

Chronic Total Occlusion of Coronary Artery Clinical Trial

Official title:
A Prospective, First in Man Study to Evaluate the Safety and Performance of the NovaCross™ Micro-catheter in (CTO) Coronary Lesions

Clinical Trial Summary

This is a prospective, non-randomized, first-in-man investigational study, to assess the safety and technical feasibility, deployment and withdrawal characteristics of the NovaCross™ micro-catheter during an interventional coronary angioplasty procedure and evaluating the CTO penetration rate.

Each study subject/patient will have a total of one (1) procedure performed for this study.

Clinical Trial Description

To be filled later ;

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

  • Chronic Total Occlusion of Coronary Artery
Clinical Trial Details
NCT number NCT01978860
Study type Interventional
Source Nitiloop Ltd.
Contact
Status Completed
Phase N/A
Start date November 2013
Completion date December 2014
View Details
See also
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