A Multicenter Registry of CorPath® 200 in PCI

A Multicenter Post-Market Registry for the Evaluation of the CorPath® 200 System Effectiveness in Percutaneous Coronary Interventions CorPath® 200 PRECISION Registry

November 22, 2017

  • Clinical Trial Information

    Trial Contact: Noel, Henry

    Trial Phone: 321.841.3686

  • IRB No: 14.009.01

    Principal Investigator: Vijaykumar S Kasi, MD

    Sub Investigators: Steiner, Mark MD

    Age Group: Adult

    Secondary Protocol No: 104-02001

    Treatment: Robotics

    Applicable Disease Sites: CAD, MI, Arteriosclerosis

    ClinicalTrials.gov ID: NCT01917682

  • Objective

    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.

  • Key Eligibility

    Cardiovascular Disease