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

Chronic Pain Clinical Trial

Official title:
Use of Dermabond in Mitigation of Spinal Cord Stimulation Trial Lead Migration

Clinical Trial Summary

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

Clinical Trial Description

Spinal Cord stimulator trials require precise placement of leads to get appropriate distribution of pain.1 Since the leads are not anchored into the tissue, migration of the leads can occur and result in suboptimal trial. Migration (or movement in the epidural space after placement) of the leads can result in up to 2.49 mm to 3.24 mm migration in the leads depending on trial length . During the 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 ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05914311
Study type Interventional
Source Wake Forest University Health Sciences
Contact Carlyle Hamsher, MD
Phone 336-716-4498
Email chamsher@wakehealth.edu
Status Recruiting
Phase N/A
Start date September 8, 2023
Completion date August 2025
View Details
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