Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
COMPLETED
NCT06295562
PHASE4

Pharmacological Treatment Targeting Endotypic Traits of Obstructive Sleep Apnea

Sponsor: China Medical University Hospital

View on ClinicalTrials.gov

Summary

This study will conduct 3 intervention trials with 44 different participants in each trial, with 22 participants will undergo in-laboratory overnight polysomnograms (PSGs) at one night of medication intervention, and the other 22 at taking placebo (contained starch) 1 h before sleep. Three medication regimens will be tested: (1) atomoxetine 80mg combined with oxybutynin 5mg; (2) venlafaxine 37.5mg; and (3) oxybutynin 5mg combined with trazodone 100mg. Endotypic traits will be estimated using the Phenotyping Using Polysomnography method. The primary outcome is the change in apnea-hypopnea index, and secondary outcomes include endotypic traits and sleep parameters.

Key Details

Gender

All

Age Range

20 Years - Any

Study Type

INTERVENTIONAL

Enrollment

45

Start Date

2024-11-05

Completion Date

2025-10-22

Last Updated

2026-04-23

Healthy Volunteers

No

Interventions

DRUG

Atomoxetine 80mg combined with oxybutynin 5mg

Atomoxetine 80mg combined with oxybutynin 5mg

DRUG

Venlafaxine 37.5mg

Venlafaxine 37.5mg

DRUG

oxybutynin 5mg combined with trazodone 100mg

oxybutynin 5mg combined with trazodone 100mg

DRUG

Placebo

Placebo tablet

Locations (1)

China Medical University Hospital

Taichung, Taiwan