Chronic Total Occlusion Percutaneous Coronary Intervention (CTO-PCI Study)
Chronic Total Occlusion Percutaneous Coronary Intervention (CTO-PCI Study)
Sponsor: Vascular Solutions LLC
Enrolling: Male and Female Patients
IRB Number: AAAS5607
U.S. Govt. ID: NCT03988166
Contact: Kate Dalton: 347-514-3366 / keb2114@cumc.columbia.edu
Additional Study Information: A study evaluating the placement of any guidewire beyond complex narrowed arteries that are relatively common in patients undergoing ballon angioplasty (a procedure where a balloon is used to stretch open narrowed arteries). At least one Teleflex guidewire and at least one Turnpike catheter is used. The guidewires and catheters that are being studied are for the intended use of facilitating the safe and effective crossing of coronary arteries that are blocked and placement of conventional guidewires beyond the narrowed artery. The data captured in this study will be used to support U.S. Food and Drug Administration (FDA) 510(k) clearance for Chronic Total Occlusion (CTO) indications.
This study is closed
Investigator
Dimitrios Karmpaliotis, MD
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For more information, please contact:
Kate Dalton
keb2114@cumc.columbia.edu
347-514-3366