Endotype DIrected Treatment for OSA in Down Syndrome

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age6+
SponsorUniversity of Arizona

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

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)

MAO inhibitor use

Urinary retention

Seizure disorder

Trial design

Design model

Parallel

Treatments tested in this trial

  • ato-oxy

    Drug

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

  • Oxygen

    Drug

    Oxygen via nasal cannula used nightly

Treatment groups

200 Participants
are divided into 2 treatment groups
Group A: Uniform therapy (ato-oxy)Active comparator 1 intervention
Group B: Endotype Directed TreatmentExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

obstructive apnea-hypopnea index (oAHI)

change in number of obstructive apneas and hypopneas per hour on polysomnography from baseline. Decreased oAHI indicates better outcome.

Time frame
12 months

Secondary outcomes

1

Change in caregiver Pediatric Quality of Life (PedsQL) score from baseline

Change in caregiver reported quality of life as measured by PedsQL, higher scores indicate better outcome.

Time frame
12 months
2

Change in Paired Associate Learning test total adjusted errors from baseline

Change in Paired Associate Learning test total errors (a measure of memory) from baseline. Fewer errors indicate better outcome

Time frame
12 months

Other outcomes

1

Change in processing speed (Arizona Memory Assessment for Preschoolers and Special Populations [A-MAP] task) from baseline.

This is a computerized cognitive assessment. Faster processing speed indicates better outcome.

Time frame
12 months
2

Change in total IQ (Kaufman Brief Intelligence Test 2) from baseline

Higher IQ indicates better outcome

Time frame
12 months
3

Change in non-verbal IQ (Kaufman Brief Intelligence Test 2) from baseline

Higher IQ indicates better outcome

Time frame
12 months
4

Change in verbal IQ (Kaufman Brief Intelligence Test 2) from baseline

Higher IQ indicates better outcome

Time frame
12 months

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Arizona

Lead sponsor

Patient-Centered Outcomes Research Institute

Collaborator