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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04186078
Other study ID # 19071511050
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 11, 2019
Est. completion date December 2046

Study information

Verified date November 2023
Source Seoul National University Hospital
Contact Jaeyoung Cho, M.D.
Phone +82-2-2072-2503
Email apricot6@snu.ac.kr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Sleep-disordered breathing including obstructive sleep apnea (OSA) is an extremely common medical disorder associated with important morbidity. The purpose of this study is to understand the clinical features and course of patients with sleep apnea in Korea. Participants who are suspected of sleep apnea due to symptoms such as snoring, witnessed apneas, waking up with a choking sensation, excessive sleepiness, non-restorative sleep, difficulty initiating or maintaining sleep, fatigue or tiredness, and morning headache will be prospectively recruited at the outpatient clinic of Seoul National University Hospital. After polysomnography (PSG) or respiratory polygraphy, patients with sleep apnea including OSA and central sleep apnea (CSA) will be followed regularly. Participants not having sleep apnea (apnea-hypopnea index < 5/hour) will only have a baseline visit. For only participants with the informed consent of donating blood, their blood samples will be collected and stored in the Seoul National University Hospital-Human Biobank (SNUH-HUB).


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date December 2046
Est. primary completion date December 2045
Accepts healthy volunteers
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria: - Participants who are suspected of sleep apnea due to symptoms such as snoring, witnessed apneas, waking up with a choking sensation, excessive sleepiness, non-restorative sleep, difficulty initiating or maintaining sleep, fatigue or tiredness, and morning headache Exclusion Criteria: - None

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Other Change of FEV1 and FVC in patients with OSA Change of forced expiratory volume in 1 s (FEV1) and forced vital capacity (FVC) in patients with OSA Median follow up of 5 years
Primary The number of participants with adherence to positive airway pressure (PAP) therapy PAP adherence is defined as the use of PAP therapy for =4 h/night on =70% of nights Median follow up of 2 years
Secondary The number of deaths The number of deaths Median follow up of 15 years
Secondary The cause of death The cause of death Median follow up of 15 years
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