COMPLETED

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

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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

Official Title

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

Quick Facts

Study Start:2023-09-08
Study Completion:2025-03-05
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT05914311

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * age greater than 18
  2. * having a spinal cord stimulator trial lead placement done
  3. * lead placement to be done in the thoracic spine area
  1. * dermabond allergy
  2. * inability to place 2 leads in subject
  3. * lead placement not in thoracic spine

Contacts and Locations

Principal Investigator

Carlyle Hamsher, MD
PRINCIPAL_INVESTIGATOR
Wake Forest University Health Sciences

Study Locations (Sites)

Wake Forest University Health Sciences
Winston-Salem, North Carolina, 27157
United States

Collaborators and Investigators

Sponsor: Wake Forest University Health Sciences

  • Carlyle Hamsher, MD, PRINCIPAL_INVESTIGATOR, Wake Forest University Health Sciences

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-09-08
Study Completion Date2025-03-05

Study Record Updates

Study Start Date2023-09-08
Study Completion Date2025-03-05

Terms related to this study

Keywords Provided by Researchers

  • Spinal Cord Stimulation (SCS)
  • chronic pain
  • stimulator

Additional Relevant MeSH Terms

  • Chronic Pain