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Optical Coherence Tomography Comparison of Neointimal Coverage Between CRE8 DES and BMS — DEMONSTRATE  

Stable Angina Clinical Trial

Official title:
Randomized Comparison Between a DES and a BMS to Assess Neointimal Coverage by OCT Evaluation

Clinical Trial Summary

The purpose of the study is to demonstrate the non-inferiority of Cre8 (CID) Drug Eluting Stent, studied 3 months after implant, compared to Vision/Multilink8 Bare Metal Stent (Abbott) studied at 1 month, in terms of neointimal coverage, determined by Optical Coherence Tomography (OCT), as percentage of cross-sections with RUTTS (Ratio of Uncovered to Total Stent Struts Per Cross Section) score ≤ 0.3.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01543373
Study type Interventional
Source CID - Carbostent & Implantable Devices
Contact
Status Completed
Phase N/A
Start date January 2012
Completion date April 2014
View Details
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