DRKS00018351CompletedNot Applicable
Validity of device-internal AHI detection during OSA therapy with regard to its application in telemonitoring - Tele-AHI
Fachkrankenhaus Kloster Grafschaft GmbH0 sites136 target enrollmentStarted: February 12, 2020Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 136
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Observational
Eligibility Criteria
- Ages
- 18 Years to one (—)
- Sex
- All
Inclusion Criteria
- •Polysomnographic or polygraphic control of a device based sleep apnoea therapy with devices of the types AirSense 10 Autoset, AirSense 10 Elite, AirSense 10 Autoset for Her, SOMNObalance, SOMNOsoft 2 oder prismaSMART
Exclusion Criteria
- •Mask leakage >25L/min, therapy duration during recording time <4h, if a nasal mask was used: mouth leakage time >10% of therapy duration
Investigators
Similar Trials
Completed
Not Applicable
Validation of novel inspection method detecting autofluorescence from eyecataract with diabetic retinopathy, cataract without diabetic retinopathyJPRN-UMIN000011110Department of Ophthalmology, Tohoku University Graduate School of Medicine120
Not yet recruiting
Unknown
To assess the effectiveness of IASTM and Cupping Therapy on Hamstring muscle in cricket bowlers.CTRI/2023/05/052261TILAK KHANA
Not yet recruiting
Not Applicable
Clinical study on the detection system for intraoperative sentinel lymph node used to ICG in Gastric Cancergastric cancerJPRN-UMIN000006091niversity of Tokushima100
Not yet recruiting
Not Applicable
Validation study of non-invasive signal analysis for presumption of balance of an intestinal flora by the human studyEnteropathyJPRN-UMIN000027688Tokushima University140
Active, not recruiting
Not Applicable
The roles of impulse oscillometry in detection of asthma control level.TCTR20190709004Faculty of Medicine, Chiang Mai University187