Radiographic and Clinical Outcomes of PureGen in Posterior Lumbar (PLIF) and Transforaminal Interbody Fusion (TLIF)
NCT01293981 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 6
Last updated 2016-01-20
Summary
The purpose of this study is to assess the safety and efficacy of PureGen Osteoprogenitor Cell Allograft in patients undergoing Posterior Lumbar or Transforaminal Interbody Fusion.
Conditions
- Lumbar Degenerative Disc Disease
Interventions
- BIOLOGICAL
-
PureGen Osteoprogenitor Cell Allograft
PureGen Osteoprogenitor Cell Allograft.
Sponsors & Collaborators
-
Alphatec Spine, Inc.
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2011-02-28
- Primary Completion
- 2012-01-31
Countries
- United States
Study Locations
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