RECRUITING

Recording of Intraoperative Spinal Cord Stimulation and Monitoring

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

Opioid overdose suppresses brainstem respiratory circuits, causes apnea, and may result in death. Epidural electrical stimulation (EES) at the cervical spinal cord facilitated motor activity in rodents and humans, and we hypothesized that EES of the cervical spinal cord could antagonize opioid-induced respiratory depression in humans. In this study, we will stimulate the spinal cord during surgery and assess its effects on respiratory function in human patients.

Official Title

Recording of Intraoperative Spinal Cord Stimulation and Monitoring

Quick Facts

Study Start:2011-01-21
Study Completion:2027-01-22
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05356286

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. * Any patients undergoing brain or spinal cord surgery where spinal neuromonitoring is utilized.
  1. * none

Contacts and Locations

Study Contact

Daniel Lu, MD
CONTACT
310/825/4321
dclu@mednet.ucla.edu

Study Locations (Sites)

University of California, Los Angeles
Los Angeles, California, 90095
United States

Collaborators and Investigators

Sponsor: University of California, Los Angeles

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 Date2011-01-21
Study Completion Date2027-01-22

Study Record Updates

Study Start Date2011-01-21
Study Completion Date2027-01-22

Terms related to this study

Additional Relevant MeSH Terms

  • Cervical Stenosis
  • Disk, Herniated
  • Spondylosis