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Safety and Efficacy Study of Healos as a Bone Replacement to Treat Degenerative Disc Disease

Degenerative Disc Disease Clinical Trial

Official title:
A Prospective, Multicenter, Randomized Study Comparing the Use of HEALOS® to Autograft in a Transforaminal Lumbar Interbody Fusion (TLIF) Approach

Clinical Trial Summary

The purpose of this study is to determine the safety and effectiveness of HEALOS compared with autograft using the transforaminal lumbar interbody fusion (TLIF) method.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00316121
Study type Interventional
Source Advanced Technologies and Regenerative Medicine, LLC (ATRM)
Contact
Status Completed
Phase Phase 3
Start date April 2006
View Details
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