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RECRUITING
NCT06287736
NA

Spinal Cord Stimulation and Small Fiber Peripheral Neuropathy

Sponsor: Ohio State University

View on ClinicalTrials.gov

Summary

This is a prospective randomized control trial. Participants enrolled into the study will be randomized into one of three groups, two of which are treatment groups and the third is a control group. A time course of measurements before and after spinal cord stimulation (SCS) treatment (where applicable) will assess pain, DPN severity, small fiber nerve activity, and metabolic health markers.

Official title: A Novel Neuromodulation Approach to Target Small Fiber Neuropathy Early in Diabetes and Measure Functional Recovery

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2024-04-17

Completion Date

2027-12-31

Last Updated

2025-07-22

Healthy Volunteers

No

Interventions

DEVICE

Spinal Cord Stimulator Implantation (SCS)

Spinal cord stimulator implantation is broken up into two parts. The first part involves placement of temporary SCS leads for a one-week trial. If the participants respond favorably to the SCS, then they will undergo the second part and the device is implanted

Locations (1)

The Ohio State University Wexner Medical Center

Columbus, Ohio, United States