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Clinical Trial Summary

The purpose of this study is to compare the effectiveness of peripheral nerve stimulation utilizing a subcutaneous lead implant technique (SQS) plus optimized medical management (OMM) versus OMM alone in patients suffering from back pain due to Failed Back Surgery Syndrome (FBSS).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01711619
Study type Interventional
Source MedtronicNeuro
Contact
Status Terminated
Phase N/A
Start date November 2012
Completion date February 2016

See also
  Status Clinical Trial Phase
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Recruiting NCT04244669 - Impact of the SCS With Different Waveforms Over the Quality of Life (SCS-Quality) N/A
Completed NCT02974101 - AdaptiveStim Objectifying Subjective Pain Questionnaires N/A
Terminated NCT01990287 - SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study N/A
Completed NCT03702010 - Spinal Cord Stimulation in Patients With Post-Laminectomy Syndrome in Testing Phase N/A