RECRUITING

Drug-Induced Sleep Endoscopy for Upper Airway Evaluation in Obstructive Sleep Apnea

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

Prospective, interventional cohort study of drug-induced sleep endoscopy (DISE) to evaluate the upper airway in a cohort of obstructive sleep apnea (OSA) surgical patients. This study has investigated the reliability of this technique, demonstrating moderate-substantial interrater and test-retest reliability. This research has also compared DISE findings to those of the lateral cephalogram X-ray and examined DISE findings in individuals who have not responded to previous sleep apnea surgery. These papers have been published and available through PubMed. Additional research is ongoing, with examination of DISE findings, comparison to other evaluation techniques, and the association between DISE findings and surgical outcomes.

Official Title

Drug-Induced Sleep Endoscopy for Upper Airway Evaluation in Obstructive Sleep Apnea

Quick Facts

Study Start:2004-02
Study Completion:2030-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT00695214

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. * Adult patients with OSA considering surgical treatment
  1. * Minors
  2. * Pregnant women
  3. * Patients unable to provide informed consent in English themselves
  4. * Prisoners
  5. * Allergy to propofol, soybean oil, egg lecithin or glycerol
  6. * Other contraindication to use of propofol (decision of anesthesiologist or otolaryngologist.)

Contacts and Locations

Study Contact

Eric J Kezirian, MD, MPH
CONTACT
4242596559
ekezirian@mednet.ucla.edu

Principal Investigator

Eric J Kezirian, MD, MPH
PRINCIPAL_INVESTIGATOR
University of California, Los Angeles

Study Locations (Sites)

UCLA Santa Monica Medical Center
Santa Monica, California, 90401
United States

Collaborators and Investigators

Sponsor: University of California, Los Angeles

  • Eric J Kezirian, MD, MPH, PRINCIPAL_INVESTIGATOR, 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 Date2004-02
Study Completion Date2030-06

Study Record Updates

Study Start Date2004-02
Study Completion Date2030-06

Terms related to this study

Keywords Provided by Researchers

  • Obstructive Sleep Apnea
  • Propofol
  • Sleep Endoscopy

Additional Relevant MeSH Terms

  • Sleep Apnea, Obstructive