TerminatedNot Applicable

CARES Lumbar Artificial Disc Registry

Stopped: Low enrollment and follow-up data on enrolled patients.

120 participantsStarted 2007-05

Plain-language 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.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Key Inclusion Criteria: * Treated with the lumbar TDR. * Signed IRB approved consent document. Key Exclusion Criteria: * None known.

What they're measuring

Change in Oswestry Disability Index (ODI) Score

Timeframe: 3, 6, 12, 24, 36, 48, and 60 months post operative

Trial details

NCT IDNCT02139527

SponsorDePuy Spine

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2009-08

View on ClinicalTrials.gov More Lumbar Degenerative Disc Disease trials