Retrospective Chart Review to Assess Outcomes in Subjects That Received MAGNIFUSE® in the Posterolateral Lumbar Spine
NCT02684045 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 76
Last updated 2017-08-21
Summary
The purpose of this chart review is to assess outcomes in subjects that received MAGNIFUSE in the posterolateral lumbar spine at 1 or 2 continuous levels from L1-S1.
Conditions
- Subjects Received MAGNIFUSE in Posterolateral Lumbar Spine
Sponsors & Collaborators
-
Medtronic Spinal and Biologics
lead INDUSTRY
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-03-01
- Primary Completion
- 2017-08-15
- Completion
- 2017-08-15
Countries
- United States
Study Locations
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