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ENROLLING BY INVITATION
NCT07016581

Optimal Duration of Spinal Cord Stimulation Trial Procedure: Length and Diagnostic Accuracy

Sponsor: University of Maryland, Baltimore

View on ClinicalTrials.gov

Summary

This study aims to find out the optimal duration (in days) needed for a spinal cord stimulator (SCS) trial procedure for treating chronic pain. While shorter trial periods could lower risks like infections or bleeding (especially for patients who need to stop blood thinners), patients also need sufficient time to achieve meaningful pain and function relief, and to report willingness to proceed to permanent implantation. Unfortunately, the optimal duration of an SCS trial procedure is not currently known. We aim to explore this optimal duration across a multi-center study by studying daily surveys completed across the duration of SCS trial procedures.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

100

Start Date

2023-06-05

Completion Date

2026-12

Last Updated

2025-06-13

Healthy Volunteers

No

Conditions

Interventions

DIAGNOSTIC_TEST

Daily survey

All patients undergoing an spinal cord stimulation trial procedure (which will be conducted in accordance to standard clinical practices per site) will be given daily surveys to assess their analgesic and functional benefit.

Locations (4)

University of Maryland

Baltimore, Maryland, United States

Mayo Clinic

Rochester, Minnesota, United States

Ohio State University

Columbus, Ohio, United States

MD Anderson Cancer Center

Houston, Texas, United States