RECRUITING

Pulse-Width Modulation

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

The overarching aim of this project is to modulate the pulse-width during stimulation of pedicle screws and record the response thresholds associated with each PWM setting. During this initial phase of the investigation, no further data will be collected.

Official Title

Pulse-width Modulation During Pedicle Screw Stimulation

Quick Facts

Study Start:2023-12-01
Study Completion:2027-06-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06120231

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. * A patient will be eligible for study participation once they have been booked for a surgery involving pedicle screw placement and intraoperative neuromonitoring.
  1. * The study excludes neonates, minors, pregnant women, prisoners and cognitively impaired patients.

Contacts and Locations

Study Contact

Beverly Allen, BS
CONTACT
6036179909
Beverly..A.Allen@hitchcock.org

Principal Investigator

Linton Evans, Dr.
PRINCIPAL_INVESTIGATOR
Dartmouth-Hitchcock Medical Center

Study Locations (Sites)

Dartmouth-Health
Lebanon, New Hampshire, 03677
United States

Collaborators and Investigators

Sponsor: Dartmouth-Hitchcock Medical Center

  • Linton Evans, Dr., PRINCIPAL_INVESTIGATOR, Dartmouth-Hitchcock Medical Center

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 Date2023-12-01
Study Completion Date2027-06-01

Study Record Updates

Study Start Date2023-12-01
Study Completion Date2027-06-01

Terms related to this study

Additional Relevant MeSH Terms

  • Spinal Fusion
  • Spinal Stenosis