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DESolve® X-Pand Global Post Market Registry — X-Pand  

Coronary Artery Stenosis Clinical Trial

Official title:
X-Pand is Intended to Use the DESolve Scaffold System in Treatment of CAD Patients, by Including "Real World" Use of the DESolve Scaffold Over a Broad Spectrum of Geographies, A Wide Variety of Practicing Clinicians & A Minimum Degree Of Selection Criteria

Clinical Trial Summary

The X-Pand Registry is intended to facilitate analysis of acute & long-term safety as well as treatment outcomes with DESolve in patients with CAD.

Clinical Trial Description

The Xpand Registry is a single-arm, multi-center, clinical Follow up study of patients with significant coronary stenosis who are treated with a commercially available DESolve Scaffold. The Registry is an observational study. The patients should be treated according to the current DESolve IFU, professional societies guidelines & internal hospital guidelines. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02453035
Study type Observational [Patient Registry]
Source Elixir Medical Corporation
Contact
Status Terminated
Phase
Start date May 13, 2015
Completion date April 30, 2017
View Details
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