Recruiting

Ato-Oxy & Oxygen

Sponsor:

University of Arizona

Code:

NCT07280468

Conditions

Obstructive Sleep Apnea (OSA)

Down Syndrome

Eligibility Criteria

Sex: All

Age: 6+

Healthy Volunteers: Not accepted

Interventions

ato-oxy

Oxygen

Study Details

Brief summary:

Down syndrome is the most common genetic cause of intellectual disability. People with Down syndrome often have obstructive sleep apnea (OSA), a condition where people have difficulties with breathing while asleep. OSA can lead to poor sleep, worse quality of life, behavior problems and more difficulties with thinking ("cognitive impairment"). Current treatments for OSA in people with Down syndrome are not very effective or require surgery. The combination of 2 medications, atomoxetine and oxybutynin ("ato-oxy") is a promising treatment for OSA in people with Down syndrome, but ato-oxy does not work for everyone with Down syndrome. Similarly, oxygen is effective for OSA in some people, but does not work for everyone. This study will evaluate the use a precision medicine approach to increase the effectiveness of OSA treatment in people with Down syndrome. The study will compare two groups. In the first group, everyone will be treated with ato-oxy. In the second group, a precision medicine approach will be used to assign participants to either ato-oxy or oxygen therapy, based on the specific reasons they have OSA.

The research team will enroll 200 children (age 6-17 years old) and adults with Down syndrome and OSA from five sites across the country. Half of participants will randomly receive ato-oxy while the other will receive either oxygen or ato-oxy dependent upon which treatment would be expected to work better for them. The research team will measure OSA severity, quality of life, behavior and cognition at the start of the study and after 12 months of treatment for every participant. The study will also track any treatment side effects for each treatment group.

Conditions

Obstructive Sleep Apnea (OSA)

Down Syndrome

Study ID

NCT07280468

Start date

Mar 14, 2026

Status verified date

Sep, 2026

Completion date

Jan, 2030

Anticipated

Primary completion date

Jan, 2030

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 6+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Age 6 years or older
2. Down syndrome diagnosis
3. Any gender or ethnicity
4. Adults without a legally authorized representative must have a caregiver/support person that can co-sign consent and complete study questionnaires.

Exclusion Criteria:

1. Currently using and adherent to PAP therapy (>4 hours per night for 70% of nights in the past 30 days based on device download or parent/caregiver report)
2. MAO inhibitor use
3. Urinary retention
4. Seizure disorder
5. Untreated or inadequately treated hypothyroidism
6. Significant traumatic brain injury
7. Not cleared to participate in the study by their cardiologist for individuals with congenital heart disease requiring follow up with cardiology at least once in the past year
8. History of current, untreated depression
9. History of liver disease (not including metabolic dysfunction-associated steatotic liver disease)
10. 3+ or greater tonsillar hypertrophy (for children only, no restriction for adults)

Study Design

Enrollment

200 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

active comparator: Uniform therapy (ato-oxy)

All participants receive the combination of atomoxetine and oxybutynin (ato-oxy) once nightly

experimental: Endotype Directed Treatment

Participants receive either atomoxetine and oxybutynin (ato-oxy) or oxygen nightly. Participants receive the treatment expected to be most beneficial to them based on their baseline sleep study and OSA characteristics (OSA endotype).

Interventions

ato-oxy

0.5 mg/kg (max 40 mg) of atomoxetine and 5mg oxybutynin taken nightly.

Oxygen

Oxygen via nasal cannula used nightly

Primary outcome measure

  • obstructive apnea-hypopnea index (oAHI) [ Time Frame: 12 months ]

Central Contacts and Locations

Central contacts

Natalie Provencio-Dean

520-403-6165nataliep@arizona.edu

Locations

University of Arizona

Recruiting

Tucson, Arizona, United States, 85724

Contacts

Natalie Provencio-Dean

520-403-6165nataliep@arizona.edu

University of California San Diego

Recruiting

San Diego, California, United States, 92123

Contacts

Principal Investigator:

Rakesh Bhattacharjee

University of Miami

Recruiting

Miami, Florida, United States, 33136

Contacts

Principal Investigator:

Ignacio Tapia

Advocate Medical Group Adult Down Syndrome Center

Recruiting

Park Ridge, Illinois, United States, 60068

Contacts

Principal Investigator:

Brian Chicoine

Children's Hospital of Philadelphia

Recruiting

Philadelphia, Pennsylvania, United States, 19104

Contacts

Principal Investigator:

Chris Cielo

More Information

Sponsor

University of Arizona

Last update posted

Sep 3, 2026

Last verified

Sep, 2026

Keywords

  • Down syndrome
  • obstructive sleep apnea
  • ato-oxy
  • precision medicine
  • oxygen
  • atomoxetine
  • oxybutynin

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by University of Arizona on 2026-09-03.