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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03890549
Other study ID # 201801799B0
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date April 1, 2019
Est. completion date December 1, 2020

Study information

Verified date December 2018
Source Chang Gung Memorial Hospital
Contact YUAN-CHIEH YEH, Doctor
Phone 24313131
Email b9005030@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to validate the downloadable mobile snore applications by polysomnography.


Description:

Obstructive sleep apnea(OSA) is characterized by multiple episodes of upper airway collapse during sleep and considered as a major health issue worldwide due to comorbidity with obesity, hypertension, diabetes and more advanced cardiovascular diseases. The noisy sounds of snoring caused by OSA bother bed partner sleepless and lead to long-term health problems. Mobile snore applications are convenient and accessible for patients to monitor the progress of OSA by themselves, but there are no reliable PSG-validated applications.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date December 1, 2020
Est. primary completion date August 31, 2020
Accepts healthy volunteers No
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- Willing to sign inform consent with aged more than 20 years old

- Mild to moderate OSA, AHI (apnea-hypopnea index) < 30

Exclusion Criteria:

- Significant lung disease

- Skeletal facial framework problems

- Central apnea

- Receiving acupuncture in recent 2 weeks

- Taking hypnotic drugs

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
SnoreLab (smart phone application for snoring recording)
The investigators selected 3 appropriate downloadable smart phone applications for snoring recording and make validation with the golden standard of polysomnography.

Locations

Country Name City State
Taiwan Keelung Chang Gung Memorial Hospital Keelung

Sponsors (1)

Lead Sponsor Collaborator
Chang Gung Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary snore time snoring time during sleep accessed by PSG and smart phone applications through study completion during sleep, each sleep cycle about 6-8 hours
Primary snore counts snoring counts during sleep accessed by PSG and smart phone applications through study completion during sleep, each sleep cycle about 6-8 hours
Primary snore sound snoring sound during sleep accessed by PSG and smart phone applications through study completion during sleep, each sleep cycle about 6-8 hours
Primary sleep time total sleep time accessed by PSG and smart phone applications through study completion during sleep, each sleep cycle about 6-8 hours
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