NeoVas Bioresorbable Coronary Scaffold Registry Study

Status Active, not recruiting

Clinical Trial Summary

The NeoVas Bioresorbable Coronary Scaffold Registry Trial is a prospective, multi-center, single arm registry trial based on the NeoVas FIM study which verified the safety and effectiveness of NeoVas initially. This study is to evaluate the safety and effectiveness of NeoVas sirolimus-eluting bioresorbable coronary scaffold in the treatment of patients with de novo coronary lesion.

Clinical Trial Description

Approximately 825 subjects will be enrolled and receive NeoVas BCS(Lepu Medical Technology (Beijing) Co.,Ltd). Subjects will have clinical follow-up at 30, 90, 180 and 270 days and at 1,2,3,4 and 5 years. The primary endpoint is target lesion failure(TLF) at 1 year follow-up. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02305472
Study type	Interventional
Source	Lepu Medical Technology (Beijing) Co.,Ltd
Contact
Status	Active, not recruiting
Phase	N/A
Start date	November 2014
Completion date	September 2020

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