CARES Lumbar Artificial Disc Registry

DePuy Synthes

Status: Terminated

Conditions: Lumbar Degenerative Disc Disease

Treatments: Device: Total Disc Replacement

Study type: Observational

Funder types: Industry

Identifiers

NCT02139527

06-CAD-01

Details and patient eligibility

About

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

Full 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.

Enrollment: 120 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Key Inclusion Criteria:

• Treated with the lumbar TDR.
• Signed IRB approved consent document.

Key Exclusion Criteria:

• None known.