Study Using the SpinalStim Device Following Lumbar Fusion Surgery

Completed

Conditions studied: Lumbar Spine Degeneration

In brief

This study examines the effect of adjunctive use of the SpinalStim bone growth stimulator on lumbar fusion rate in high risk subjects who have had lumbar fusion surgery. All participants will wear the bone growth stimulator for a minimum of 2 hours/day for 6 months.

Key facts

Study ID
NCT03176303
Run by
Orthofix Inc.
People needed
206
Starts
2017-06-28
Expected to finish
2021-07-12
Last updated by the study team
2022-09-16

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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