Actively Recruiting

Phase 4
Age: 6Years +
All Genders
NCT07280468

Endotype DIrected Treatment for OSA in Down Syndrome

Led by University of Arizona · Updated on 2026-04-07

200

Participants Needed

5

Research Sites

198 weeks

Total Duration

On this page

Sponsors

U

University of Arizona

Lead Sponsor

P

Patient-Centered Outcomes Research Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

Official Title

Endotype DIrected Treatment for OSA in Down Syndrome

Who Can Participate

Age: 6Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 6 years or older
  • Diagnosis of Down syndrome
  • Any gender or ethnicity
  • Adults without a legally authorized representative must have a caregiver or support person able to co-sign consent and complete study questionnaires
Not Eligible

You will not qualify if you...

  • Currently using and adherent to positive airway pressure (PAP) therapy (more than 4 hours per night for 70% of nights in the past 30 days)
  • Use of MAO inhibitors
  • Urinary retention
  • Seizure disorder
  • Untreated or inadequately treated hypothyroidism
  • Significant traumatic brain injury
  • Not cleared by cardiologist if having congenital heart disease with follow-up in past year
  • Current untreated depression
  • History of liver disease (excluding metabolic dysfunction-associated steatotic liver disease)
  • 3 or more tonsillar hypertrophy (children only)

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 5 locations

1

University of Arizona

Tucson, Arizona, United States, 85724

Actively Recruiting

2

University of California San Diego

San Diego, California, United States, 92123

Not Yet Recruiting

3

University of Miami

Miami, Florida, United States, 33136

Not Yet Recruiting

4

Advocate Medical Group Adult Down Syndrome Center

Park Ridge, Illinois, United States, 60068

Not Yet Recruiting

5

Children's Hospital of Philadelphia

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

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Research Team

N

Natalie Provencio-Dean

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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