Completed NA INTERVENTIONAL 6-arm
NCT00295009
Safety and Effectiveness Study of Prodisc to Spinal Fusion Surgery (PDL)
A Multi-Center, Prospective, Randomized, Controlled Clinical Trial Comparing the Safety and Effectiveness of ProDisc to Spinal Fusion Surgery in the Treatment of Discogenic Pain Associated With DDD in the Lumbosacral Spine
Sponsor: Synthes USA HQ, Inc.
Conditions
Spinal Diseases
Interventions
ProDisc Spinal Fusion
Last updated: Jul 31, 2014 Started: Sep 30, 2001 Primary completion: Apr 30, 2011 Completion: Apr 30, 2011
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.
A NA clinical study on Spinal Diseases, this trial is completed. The trial is conducted by Synthes USA HQ, Inc. and has accumulated 0 data snapshots since 2001. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.
Change History
No change history available.
Eligibility Summary
No eligibility information available.
Contact Information
Sponsor contact:
- Synthes USA HQ, Inc.
Data source: Synthes USA HQ, Inc.
For direct contact, visit the study record on ClinicalTrials.gov .
Study Locations
No location information available.