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RecruitingNCT07302685TOSAUpdated Dec 24, 2025

The Taiwan OSA Study

An observational study in Obstructive Sleep Apnea, sponsored by China Medical University Hospital. Recruiting at 1 site in Taiwan. Open to participants aged 0 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-12-24.

Sponsored by China Medical University Hospital · Observational

From the registry’s dates

  • Started Apr 2020; still recruiting 6 years 5 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
7,000
Ages
0 Years and older
Sex
All
01

Study summary

We will prospectively recruit 7000 OSA patients referred to the sleep center or China Medical University Hospital between 2020 and 2027. Polysomnographic (PSG) study data, clinical features, and health data from the National Health Insurance Research Database will be linked. Endotypic traits will be determined by PSG study parameters. The associations between clinical features, endotypic traits, and health outcome will be examined. Some patients will be invited to receive lung function tests, blood serum tests, blood gas tests, and cognitive function tests.

02

Conditions studied

  • Obstructive Sleep Apnea
03

In context

Sleep Apnea, Obstructive

2,198 studies on the registry are indexed under Sleep Apnea, Obstructive; 470 are open to participants now.

This study's planned enrollment of 7,000 is above the median of 104 across 648 observational studies indexed under Sleep Apnea, Obstructive.

Browse Sleep Apnea, Obstructive studies →

Lead sponsor

China Medical University Hospital is the lead sponsor of 464 studies on the registry; 116 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
0 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Patients who are referred to China Medical University Hospital sleep center by physicians

Inclusion criteria

  • patients who are referred to China Medical University Hospital sleep center by physicians

Exclusion criteria

Exclusion Criteria:

-Individuals unable to complete at least 6 hours of PSG examination

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
7,000 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Cohort Label
06

What researchers measure

Primary outcomes

  1. Health outcome

    Registered diagnosis in the National Health Insurance Database

    Time frame: Within 20 years from the date of the PSG examination

Secondary outcomes

  1. Sleep quality

    Pittsburgh Sleep Quality Index (PSQI) ranges from 0 (better) to 21 (worse).

    Time frame: Baseline

  2. Daytime sleepiness

    Epworth Sleepiness Scale ranges from 0 (better) to 24 (worse)

    Time frame: Baseline

  3. Sleep quality

    Basic Nordic Sleep Questionnaire,a higher Basic Nordic Sleep Questionnaire score indicates worse outcomes

    Time frame: Baseline

  4. Sleep quality

    Munich Chronotype Questionnaire

    Time frame: Baseline

07

Study locations

1 of 1 sites recruiting
  • China Medical University Hospital
    Taichung, Taiwan 404, Taiwan
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 24, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07302685
Lead sponsor
China Medical University Hospital
Responsible party
Wan-Ju Cheng (Doctor, China Medical University Hospital) — Principal investigator
First posted
Dec 24, 2025
Start date
Apr 10, 2020
Primary completion
Feb 28, 2032 (estimated)
Completion
Feb 28, 2032 (estimated)
Last update
Dec 24, 2025

Study contacts

Wan-Ju Cheng, Doctor
Contact
s871065@gmail.com
+1872 +886422052121

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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