Safety and Effectiveness Study of Prodisc to Spinal Fusion Surgery

NACompletedINTERVENTIONAL
Enrollment

852

Participants

Timeline

Start Date

September 30, 2001

Primary Completion Date

April 30, 2011

Study Completion Date

April 30, 2011

Conditions
Spinal Diseases
Interventions
DEVICE

ProDisc

Total disc replacement with ProDisc

PROCEDURE

Spinal Fusion

A circumferential fusion will be utilized as the control group in this study. The technique will consist of an interbody fusion procedure using commercially available femoral ring allograft. A posterior lateral fusion with autogenous iliac crest bone graft, combined with pedicle screw instrumentation.

All Listed Sponsors
lead

Synthes USA HQ, Inc.

INDUSTRY

NCT00295009 - Safety and Effectiveness Study of Prodisc to Spinal Fusion Surgery | Biotech Hunter | Biotech Hunter