SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study

Stopped early · Not applicable

Conditions studied: Failed Back Surgery Syndrome, Post-Laminectomy Syndrome, Low Back Pain

In brief

The purpose of the study is to demonstrate safety and efficacy of spinal cord stimulation with peripheral nerve field stimulation for the treatment of chronic low back and leg pain.

Key facts

Study ID
NCT01990287
Run by
Abbott Medical Devices
People needed
38
Starts
2013-11-01
Expected to finish
2016-02-01
Last updated by the study team
2016-04-13

Who can join

Age: 22 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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