CARES Lumbar Artificial Disc Registry

Status Terminated

Clinical Trial Summary

The purpose of the registry is to assess outcomes following treatment with lumbar total disc replacement (TDR) in patients outside the clinical trial setting.

Clinical Trial Description

The purpose of this study is to capture outcomes associated with use of total disc replacement (TDR) in patients treated with either the CHARITE™ Artificial Disc or the PRODISC®-L Total Disc Replacement may be included in the registry. ;

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02139527
Study type	Observational [Patient Registry]
Source	DePuy Spine
Contact
Status	Terminated
Phase	Phase 4
Start date	May 2007
Completion date	August 2009

View Details

See also
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