Use of Dermabond in Mitigation of Spinal Cord Stimulation (SCS) Trial Lead Migration

Completed · Not applicable

Conditions studied: Chronic Pain

In brief

During the typical SCS trial the leads remain outside of the skin and can be prone to migration. The leads are typically secured in place with suture, tape, or a combination of both. This study will evaluate the amount of movement based on the method of being secured at the time of placement

Key facts

Study ID

NCT05914311

Run by

Wake Forest University Health Sciences

People needed

57

Starts

2023-09-08

Expected to finish

2025-02-26

Last updated by the study team

2026-06-09

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• age greater than 18
• having a spinal cord stimulator trial lead placement done
• lead placement to be done in the thoracic spine area

You may not qualify if…

• dermabond allergy
• inability to place 2 leads in subject
• lead placement not in thoracic spine

Where it is running

• Wake Forest University Health Sciences — Winston-Salem, North Carolina, United States

Full record on ClinicalTrials.gov

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