CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 57 enrolled / 57 target
Drug / intervention
Suture +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05914311
NCT05914311N/ACompletedHigh Momentum (1.7/mo)Completion was 16mo ago
CompareCT.gov

Use of Dermabond in Mitigation of Spinal Cord Stimulation Trial Lead Migration

Wake Forest University Health Sciences·interventional·Posted Jun 22, 2023·Updated Jun 9, 2026

In Brief

A clinical study evaluating Suture and Suture and Dermabond for Chronic Pain. Completed, enrolled 57 participants across 1 site.

Signals

Enrolling ahead of pace

Detailed 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

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsChronic Pain
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
202420252026
First PostedJun 22, 2023
Enrollment StartSep 8, 2023
Primary CompletionFeb 26, 2025
TodayJul 2, 2026
Enrollment to primary: 1.5 yearsPosted 3.0 years ago

Arms & Interventions

Suture Groupactive_comparator

secure one of the 2 trial leads with suture only-randomized to left or right

Device: Suture
Dermabond and Suture Groupexperimental

secure one of the 2 trial leads to be secured with both dermabond and suture-randomized to left or right

Device: SutureDevice: Suture and Dermabond

Interventions

Suturedevice

secures SCS trial leads with a suture

Suture and Dermabonddevice

secures SCS trial leads with dermabond and suture