Obstructive Sleep Apnea Clinical Trials

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Endotype DIrected Treatment for OSA in Down Syndrome

Status: Recruiting
Location: See all (5) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 6
Healthy Volunteers: f
View:

• Age 6 years or older

• Down syndrome diagnosis

• Any gender or ethnicity

• Adults without a legally authorized representative must have a caregiver/support person that can co-sign consent and complete study questionnaires.

Locations
United States
Arizona
University of Arizona
RECRUITING
Tucson
California
University of California San Diego
NOT_YET_RECRUITING
San Diego
Florida
University of Miami
NOT_YET_RECRUITING
Miami
Illinois
Advocate Medical Group Adult Down Syndrome Center
NOT_YET_RECRUITING
Park Ridge
Pennsylvania
Children's Hospital of Philadelphia
RECRUITING
Philadelphia
Contact Information
Primary
Natalie Provencio-Dean
nataliep@arizona.edu
520-403-6165
Time Frame
Start Date: 2026-03-14
Estimated Completion Date: 2030-01
Participants
Target number of participants: 200
Treatments
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).
Related Therapeutic Areas
Sponsors
Collaborators: Patient-Centered Outcomes Research Institute
Leads: University of Arizona

This content was sourced from clinicaltrials.gov