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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


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

See also
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