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Clinical Trial Summary

To collect data on the routine patterns of use, safety and effectiveness, including the clinical and technical performance of the CorPath GRX System, in the delivery and manipulation of coronary guidewires and stent/balloon catheters, and manipulation of guide catheters during PCI procedures in the first 231 patients treated with the CorPath device in Japan.


Clinical Trial Description

This is a single-arm, open-label, multi-center patient registry in Japan of the CorPath GRX System to examine its performance during PCI procedures and patient outcomes through 72 hours post-procedure or hospital discharge, whichever occurs first. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03870087
Study type Observational [Patient Registry]
Source Corindus Inc.
Contact Tina M Ridgeway, BS, RN
Phone 7578105166
Email tina.ridgeway@corindus.com
Status Not yet recruiting
Phase
Start date April 2019
Completion date November 2020

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