None listed
Conditions
Brief summary
The purpose of the current study is to determine the safety and efficacy of a neuromodulation therapy in the treatment of chronic pain. We hypothesize that this study will demonstrate safe delivery of therapy which will result in significant pain relief.
Interventions
This study uses an invasive neurostimulation device that is used for up to 24 hours per day. Duration of treatment in this study is 3-10 days. Part of the device is implanted in the patient and the device is controlled with a hand held remote. The amount of therapy used throughout the day is patient controlled.
Sponsors
Five Corners Pty Ltd
Study design
Allocation
Non-randomised trial
Primary purpose
Treatment
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Chronic pain 2. Failed conservative treatments
Exclusion criteria
Primarily axial back pain
Outcome results
None listed