Neuromodulation Parameter Efficacy
Not Applicable
Recruiting
- Conditions
- Chronic Pain
- Interventions
- Other: Stimulation parameters
- Registration Number
- NCT04933370
- Lead Sponsor
- Alberta Health Services, Calgary
- Brief Summary
The objective of this study is to determine the efficacy of neuromodulation using various stimulation paradigms in the treatment of several disorders including chronic pain.
- Detailed Description
Different stimulation parameters will be tried in a blinded fashion to compare efficacy.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
- Patients who are candidates for, and have been consented for, implantation of a neuromodulation device.
Exclusion Criteria
- Non-English speaking
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Industry standard stimulation Stimulation parameters Industry standard stimulation settings Experimental stimulation Stimulation parameters Experimental stimulation settings
- Primary Outcome Measures
Name Time Method Change in baseline pain measures 6 months Pain outcomes measured using visual analogue scale
- Secondary Outcome Measures
Name Time Method Effect of stimulation on quality of life 6 months As measured using EQ-5D-3L
Trial Locations
- Locations (1)
University of Calgary
🇨🇦Calgary, Alberta, Canada