Validation of portable sleep monitoring device in sleep breathing disorder patients

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0002098

Enrollment

200

Registered

2016-10-14

Start date

2014-07-23

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 : Execute formal polysomnography and ApneaLink Plus simultaneously and in addition, test with ApneaLink only home and compare and analyze the results respectively.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients aged 4 years or older who took sleep test for sleep related breathing disorder 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
Apnea-hypopnea index ;Risk Indicator;Unclassied Apnea Index;Obstructive Apnea Index;Central Apnea Index;Mixed Apnea Index;Oxygen desaturation index;snoring event;Respiratory disturbance index ;snoring time;hypopnea index;flow limitation	—

Countries

Korea, Republic of

Contacts

Public ContactHyun Jun Kim

Ajou University Hospital

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

Outcome results