None listed
Conditions
Brief summary
This study is a clinical audit of patients undergoing implantation of a commercially-available and TGA-approved high frequency stimulator (TGA certificate DV-2011-MC-00182-3) between 1st January 2013 and 1st February 2017 for the clinical management of pain. The study will be a two-year audit of pain scores, disability index, analgesic drug consumption and patient satisfaction after implantation of a high frequency electrical nerve stimulator. Each patient will provide their informed consent for their data to be included in the clinical audit.
Interventions
Sponsors
Eligibility
Inclusion criteria
All patients at Dr Finch’s pain practice who were implanted with a high frequency electrical nerve stimulator (Nevro high frequency stimulator and electrode leads, TGA certificate DV-2011-MC-00182-3) between 1st January 2013 and 1st February 2017 will be invited to be included in the clinical audit.
Exclusion criteria
None