Investigation of accuracy and reliability of new type sleep monitoring device(Wach-PAT) in sleep breathing disorder patients

Validation of new type sleep monitoring device(Wach-PAT 200) in sleep breathing disorder patients

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0002099

Enrollment

Registered

2016-10-14

Start date

2014-07-12

Completion date

Unknown

Last updated

2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device : Compare each test result and its accuracy and reliability by analyzing statistically, by wearing Watch-PAT and executing polysomnography simultaneously at sleep test room

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients aged 13 years or older and less than 18 years who take sleep test for sleep related breathing disorders such as snoring or apnea

Exclusion criteria

Exclusion criteria: Patients with severe diseases such as congenital malformation, disorder, etc.

Design outcomes

Primary

Measure	Time frame
sleep (minute);sleep (%);peripheral Respiratory disturbance index;peripheral Apnea-hypopnea index;Oxygen desaturation index ;Light Sleep;Deep Sleep;Rapid Eye Movement Sleep;Wake;Respiratory disturbance index;Apnea-hypopnea index;snoring time;sleep efficiency;Non-Rapid Eye Movement Sleep I;Non-Rapid Eye Movement Sleep II;Non-Rapid Eye Movement Sleep III;Rapid Eye Movement Sleep;wake	—

Countries

Korea, Republic of

Contacts

Public ContactHyun Jun Kim

Ajou University Hospital

entkhj@naver.com+82-31-219-5267

Outcome results