Last updated on December 2016

Post-Market CorPath Registry on the CorPath 200 System in Percutaneous Coronary Interventions


Brief description of study

To collect data on the routine patterns of use, safety and effectiveness, including the clinical and technical performance of the CorPath 200 System, in the delivery and manipulation of coronary guidewires and stent/balloon catheters during PCI procedures.

Detailed Study Description

This is a prospective, single-arm, open-label, multi-center patient registry of the CorPath 200 System to examine its performance during PCI procedure and patient outcomes through 72 hours post-procedure or hospital discharge, whichever occurs first.

Clinical Study Identifier: NCT01917682

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Recruitment Status: Open


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