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Clinical Trial Summary

Postmarket surveillance in terms of the safety and efficacy of Sirolimus-eluting Coroflex ISAR Stent for the treatment of "real world" patients with de-novo and restenotic lesions after stand-alone angioplasty in coronary arteries


Clinical Trial Description

The aim of the study is to assess the safety and efficacy of elective deployment of the Sirolimus-eluting Coroflex ISAR Stent for the treatment of "real world" de-novo and restenotic lesions after stand-alone angioplasty in coronary arteries of 2.0 mm up to 4.0 mm in diameter and up to 30 mm in length for procedural success and preservation of vessel patency. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02629575
Study type Observational [Patient Registry]
Source B. Braun Melsungen AG
Contact
Status Completed
Phase N/A
Start date January 2014
Completion date December 2017

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