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Clinical Trial Summary

Prospective, non-randomized, multicenter registry


Clinical Trial Description

Enrollment of up to 50 subjects with up to two de novo native coronary artery lesions measuring between 2.25 and 3.5 mm in diameter and<=34 mm in length receiving the DynamX Novolimus Eluting Coronary Bioadaptor System (CSS), with primary, interim clinical follow-up via telephone at 1 month. Follow-up will continue at 6, and 12 months. to capture cardiovascular related hospitalizations related to the study devic ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04483791
Study type Interventional
Source Elixir Medical Corporation
Contact
Status Active, not recruiting
Phase Phase 4
Start date September 30, 2020
Completion date December 2022

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