Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
3000 participants
OBSERVATIONAL
2019-04-08
2019-09-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Is the Daytime Sleepiness Based on Epworth Sleepiness Scale a Good Way to Assess Taiwanese With Suspected Obstructive Sleep Apnea.
NCT04631783
Long Term Prognosis of Taiwanese Patients With OSA
NCT02090023
Drug Induced Submental Ultrasound in Obstructive Sleep Apnea Patients
NCT03285451
Obstructive Sleep Apnea (OSA), Oral Frailty, Dysphagia, Continuous Positive Airway Pressure (CPAP)
NCT05977296
The Role of Clinical Parameters in Predicting the Severity of Obstructive Sleep Apnea
NCT00302614
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Young adult, without OSAS
20\<=Age\<40 years old, apnea-hypopnea index(AHI)\<5
Age
Age\<40 years old is chosen as the cutoff value.
Young adult, with OSAS
20\<=Age\<40 years old, AHI\>=5
Age
Age\<40 years old is chosen as the cutoff value.
OSA
The diagnosis of OSA (obstructive sleep apnea) relies on polysomnographic data showing an apnea-hypopnea index at least 5/hr with compatible symptoms.
older adult, without OSAS
Age\>=40 years old, AHI\<5
No interventions assigned to this group
older adult, with OSAS
Age\>=40 years old, AHI\>=5
OSA
The diagnosis of OSA (obstructive sleep apnea) relies on polysomnographic data showing an apnea-hypopnea index at least 5/hr with compatible symptoms.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Age
Age\<40 years old is chosen as the cutoff value.
OSA
The diagnosis of OSA (obstructive sleep apnea) relies on polysomnographic data showing an apnea-hypopnea index at least 5/hr with compatible symptoms.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Patients cannot tolerate PSG examination
* Patients cannot complete the questionnaires before and after PSG examination
20 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Taipei Veterans General Hospital, Taiwan
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
vghtpe user
Principal Investigator, Medical Doctor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Chest department, Taipei Veteran General Hospital
Taipei, , Taiwan
Countries
Review the countries where the study has at least one active or historical site.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
References
Explore related publications, articles, or registry entries linked to this study.
Chiu HY, Chou KT, Su KC, Lin FC, Liu YY, Shiao TH, Chen YM. Obstructive sleep apnea in young Asian adults with sleep-related complaints. Sci Rep. 2022 Nov 29;12(1):20582. doi: 10.1038/s41598-022-25183-5.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2018-10-002CC
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.