NCT00291018View on ClinicalTrials.gov

Safety and Efficacy Study Comparing ProDisc-C to ACDF Surgery to Treat SCDD

NACompletedINTERVENTIONAL
Enrollment

368

Participants

Timeline

Start Date

August 1, 2003

Primary Completion Date

March 1, 2015

Study Completion Date

March 1, 2015

Conditions
Symptomatic Cervical Disc Disease
Interventions
DEVICE

Total Disc Replacement

Total Disc Replacement using ProDisc-C

DEVICE

ACDF

Anterior Cervical Discectomy and Fusion

All Listed Sponsors
lead

Synthes USA HQ, Inc.

INDUSTRY

NCT00291018 - Safety and Efficacy Study Comparing ProDisc-C to ACDF Surgery to Treat SCDD | Biotech Hunter | Biotech Hunter