RECRUITING

Comparison of a Demand Oxygen Delivery

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

Conducting a randomized control trial of oxygen in children with Down syndrome to treat moderate to severe obstructive sleep apnea. The aim of the study is to conduct a comparison between the 2 methods of oxygen delivery during sleep in 15 children from Cincinnati Children's Hospital and Children's Hospital of Los Angeles. 2 polysomnographies will be performed, one with continuous flow and the second with pulse flow.

Official Title

Comparison of a Demand Oxygen Delivery to Continuous Flow for Administration of Oxygen During Sleep

Quick Facts

Study Start:2023-01-09
Study Completion:2026-12-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06609694

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:5 Years to 17 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. 1. Age 5-17 years with or without Down Syndrome (DS).
  2. 2. Children with obstructive sleep apnea (OSA) and obstructive apnea hypopnea index (OAHI) 5-40 / hour: The rationale for selecting this range of OAHI is that a large number of children with DS with this range of OSA severity are untreated for months to years. It is important to understand the response to oxygen across the spectrum of disease severity. Notably, children with severe disease are left with few options (e.g., tracheostomy).
  3. 3. Absence of clinically significant hypoxia defined as oxygen saturation \< 88% for 5 minutes or episodic desaturation to 60% as these levels would otherwise identify children eligible to routinely receive oxygen.
  1. 1. Current CPAP use with documented compliance (\> 4 hrs/ night; \> 70% of nights).
  2. 2. Oxygen saturation \< 90% at rest during wakefulness
  3. 3. Chronic daytime or nighttime use of supplemental oxygen.
  4. 4. Unable to participate in a Polysomnogram (PSG).
  5. 5. Enrolled or planning to enroll in another study that may conflict with protocol requirements or confound results in this trial.

Contacts and Locations

Study Contact

Suzie Hicks, BS
CONTACT
513-636-4944
suzie.hicks@cchmc.org

Principal Investigator

Raouf Amin, MD
PRINCIPAL_INVESTIGATOR
Children's Hospital Medical Center, Cincinnati

Study Locations (Sites)

Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio, 45229
United States

Collaborators and Investigators

Sponsor: Children's Hospital Medical Center, Cincinnati

  • Raouf Amin, MD, PRINCIPAL_INVESTIGATOR, Children's Hospital Medical Center, Cincinnati

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 Date2023-01-09
Study Completion Date2026-12-01

Study Record Updates

Study Start Date2023-01-09
Study Completion Date2026-12-01

Terms related to this study

Keywords Provided by Researchers

  • Sleep Apnea
  • Down Syndrome
  • Continuous Positive Airway Pressure (CPAP)

Additional Relevant MeSH Terms

  • Obstructive Apnea