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RECRUITING
NCT05350215
PHASE1/PHASE2

Atomoxetine and DAW2022 on OSA Severity

Sponsor: Brigham and Women's Hospital

View on ClinicalTrials.gov

Summary

Obstructive sleep apnea (OSA) is common and has major health implications but treatment options are limited. In previous research atomoxetine and oxybutynin showed promising effect at reducing OSA severity, however they reduced arousal threshold, one of the key traits responsible for OSA. Since oxybutynin was used mainly as a hypnotic, but it is burdened by several anti-cholinergic side effects, DAW2020, a hypnotic which prolonged the total sleep time in a previous trial in OSA patients, could be a better candidate to associate with atomoxetine.

Official title: Effect of Atomoxetine and DAW2022 on OSA Severity

Key Details

Gender

All

Age Range

21 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

18

Start Date

2022-06-01

Completion Date

2026-06-01

Last Updated

2026-03-03

Healthy Volunteers

No

Interventions

DRUG

Placebo oral capsule

Placebo pills for a week, 1 pill 4 hr before sleep and 1 pill 30 min before sleep

DRUG

Atomoxetine Oral Capsule [Strattera]

Atomoxetine for a week: 40 mg for 3 days 30 min before sleep, 80 mg for 4 days 30 min before sleep Simultaneous administration of DAW2020 for a week, 34 mg 4 h before sleep

Locations (1)

Brigham and Women's Hospital

Boston, Massachusetts, United States