Expired Study
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Spartanburg, South Carolina 29303


Purpose:

To determine the best parameters with various leads to cover back and leg pain and provide best pain relief


Study summary:

Prospective double-blinded trial of patients already implanted with SCS to determine which programming model best controls their back and or leg pain. Baseline visit is 2 weeks after implant. Baseline study data is collected, program #1 is started. The visit @ week 4 collects NRS and stimulator data, changes to program #2. The visit @ week 6 collect NRS and stimulator data, and starts program #3. The visit @ week 8 collects NRS and stimulator data. Subject chooses their preferred program from the previous 3 and uses that for the next 12 weeks. The visit @ week 20 collects NRS and stimulator data and final study visit information.


Criteria:

Inclusion Criteria: - spinal cord stimulator implant within last 3 weeks - NRS > 6 - at least 22 years old - patients who agree not to add or increase their pain medications during the study Exclusion Criteria: - patients with prior spinal cord stimulators - pregnancy - infusion pump - history of substance abuse or dependency in last 6 months


NCT ID:

NCT02346383


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Spartanburg, South Carolina 29303
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 24, 2017

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