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Clinical Trial Summary

The CTO-DENOVO study is a multicenter registry of consecutive patients with de novo CTO undergoing successful CTO recanalization with the use of DCB-only strategy. The primary endpoint is target lesion failure at 6 months. The secondary endpoints are: 1) late lumen loss on follow-up angiography, and 2) minimal lumen area on follow-up intravascular ultrasound.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05977842
Study type Observational
Source National Institute of Cardiology, Warsaw, Poland
Contact Maksymilian Opolski, MD
Phone +48501444303
Email mopolski@ikard.pl
Status Recruiting
Phase
Start date January 31, 2024
Completion date July 31, 2024

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