Spinal Cord Stimulation Research Study
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Limb Pain
- Sponsor
- MedtronicNeuro
- Enrollment
- 100
- Locations
- 9
- Primary Endpoint
- Numeric Pain Rating Scale (NPRS) - Cohort 1
- Status
- Terminated
- Last Updated
- last year
Overview
Brief Summary
To characterize the effects of stimulation parameters on pain relief and other cohort specific outcomes.
Detailed Description
This post market study will measure the following: * Numeric Pain Rating Scale * Satisfaction and Stimulation Assessment * Stimulation feedback * Stimulation parameters * Anatomical locations of active contacts * Stimulation thresholds * Location of paresthesia * Oswestry Disability Index * European Quality of Life 5-Dimensions * To characterize non-invasive health monitoring data
Investigators
Eligibility Criteria
Inclusion Criteria
- •22 years of age or older
- •Implanted with a Medtronic rechargeable neurostimulation system, for a labeled indication, for at least 1 month and expected longevity of neurostimulator is at least 5 months
- •Willing and able to provide signed and dated informed consent
- •Capable of comprehending and consenting in English
- •Willing and able to comply with all study procedures, including diary completion, and visits
- •Able to differentiate between pain associated with the indication for SCS implant and other types of pain
Exclusion Criteria
- •Implanted with neurostimulation system for an off-label indication
- •Currently enrolled or planning to enroll in an interventional clinical study that could potentially confound the study results
- •If female, pregnant or is of child-bearing potential and unwilling to use a medically acceptable form of birth control during the study
- •Has untreated major psychiatric comorbidity
- •Has a non-rechargeable neurostimulator where the battery longevity is not able to be estimated with the battery longevity calculator
Outcomes
Primary Outcomes
Numeric Pain Rating Scale (NPRS) - Cohort 1
Time Frame: Up to 5 months
To characterize the effect of different programmed settings on pain relief. The NPRS will be recorded once or daily over a period of time, where the subjects will rate their pain on a 11-point numeric rating scale of 0 to 10, with 0 representing 'No Pain' and 10 representing 'Worst pain imaginable'. The average overall NPRS pain score prior to the scheduled visit will be used for analysis.
Numeric Pain Rating Scale (NPRS) - Cohort 2
Time Frame: Up to 2 months
To characterize the effect of different programmed settings on pain relief. The NPRS will be recorded once or daily over a period of time, where the subjects will rate their pain on a 11-point numeric rating scale of 0 to 10, with 0 representing 'No Pain' and 10 representing 'Worst pain imaginable'. The average overall NPRS pain score prior to the scheduled visit will be used for analysis.
Numeric Pain Rating Scale (NPRS) - Cohort 3
Time Frame: Up to 3 months
To characterize the effect of different programmed settings on pain relief. The NPRS will be recorded once or daily over a period of time, where the subjects will rate their pain on a 11-point numeric rating scale of 0 to 10, with 0 representing 'No Pain' and 10 representing 'Worst pain imaginable'. The average overall NPRS pain score prior to the scheduled visit will be used for analysis.
Numeric Pain Rating Scale (NPRS) - Cohort 4
Time Frame: Up to 5 months
To characterize the effect of different programmed settings on pain relief. The NPRS will be recorded once or daily over a period of time, where the subjects will rate their pain on a 11-point numeric rating scale of 0 to 10, with 0 representing 'No Pain' and 10 representing 'Worst pain imaginable'. The average overall NPRS pain score prior to the scheduled visit will be used for analysis.
Numeric Pain Rating Scale - Cohort 5
Time Frame: Up to 5 months
To characterize the effect of different programmed settings on pain relief. The NPRS will be recorded once or daily over a period of time, where the subjects will rate their pain on a 11-point numeric rating scale of 0 to 10, with 0 representing 'No Pain' and 10 representing 'Worst pain imaginable'. The average overall NPRS pain score prior to the scheduled visit will be used for analysis.
Numeric Pain Rating Scale (NPRS) - Cohort 6
Time Frame: Up to 7 months
To characterize the effect of different programmed settings on pain relief. The NPRS will be recorded once or daily over a period of time, where the subjects will rate their pain on a 11-point numeric rating scale of 0 to 10, with 0 representing 'No Pain' and 10 representing 'Worst pain imaginable'. The average overall NPRS pain score prior to the scheduled visit will be used for analysis.
Numeric Pain Rating Scale (NPRS) - Cohort 7
Time Frame: Up to 8 months
To characterize the effect of different programmed settings on pain relief. The NPRS will be recorded once or daily over a period of time, where the subjects will rate their pain on a 11-point numeric rating scale of 0 to 10, with 0 representing 'No Pain' and 10 representing 'Worst pain imaginable'. The average overall NPRS pain score prior to the scheduled visit will be used for analysis.
Numeric Pain Rating Scale (NPRS) - Cohort 8
Time Frame: Up to 0.5 months
To characterize the effect of different programmed settings on pain relief. The NPRS will be recorded once or daily over a period of time, where the subjects will rate their pain on a 11-point numeric rating scale of 0 to 10, with 0 representing 'No Pain' and 10 representing 'Worst pain imaginable'. The average overall NPRS pain score prior to the scheduled visit will be used for analysis.
Numeric Pain Rating Scale at Enrollment (NPRS) - Cohort 9
Time Frame: Up to 1 month
To characterize the effect of different programmed settings on pain relief. The NPRS will be recorded once or daily over a period of time, where the subjects will rate their pain on a 11-point numeric rating scale of 0 to 10, with 0 representing 'No Pain' and 10 representing 'Worst pain imaginable'. The average overall NPRS pain score prior to the scheduled visit will be used for analysis.