DynamX Bioadaptor Hong Kong Registry

Status Completed

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

Coronary Artery Disease

Clinical Trial Details

NCT number	NCT04483791
Study type	Interventional
Source	Elixir Medical Corporation
Contact
Status	Completed
Phase	Phase 4
Start date	September 30, 2020
Completion date	December 31, 2022

View Details

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