Clinical Trial

Prospective Evaluation of the Optimal SCS Trial Length

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Summary
This study aims to determine the ideal length of a spinal cord stimulation (SCS) trial period by analyzing daily pain scores, patient satisfaction, and when patients decide whether to proceed with permanent implantation. The primary goal is to identify the shortest trial duration that can reliably predict SCS success. A secondary goal is to compare SCS trial outcomes with patient-reported health measures (PROMIS domains) and recommendations from the SCS E-Health Tool to evaluate how well these tools predict treatment candidacy and outcomes.
Trial Details
NCT Number NCT07709351
Lead Sponsor Ohio State University
Conditions Spinal Cord Stimulation
Enrollment 42 participants
Start Date 2026-08-28
Primary Completion 2029-08-31 (estimated)
Study Completion 2029-08-31 (estimated)
Updated on ClinicalTrials.gov 2026-07-16