Observation and evaluation of the efficacy of the ventilator LUISA (LM150TD) on respiratory insufficiency
- Conditions
- eurological diseases (e. g. neuromuscular diseases, disorders of the respiratory center) and lung damages
- Registration Number
- DRKS00023838
- Lead Sponsor
- öwenstein Medical Technology GmbH & Co. KG
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 16
Inclusion Criteria
Clinical ventilation (e. g. because of acute respiratory failure) with a clinical ventilator (different from LUISA)
Or
Change of ventilator with an clinical application equivalent to LUISA as part of therapy control
Or
Primary ventilation therapy setting
Indication for subsequent home ventilation according to corresponding guidline
Exclusion Criteria
Data for primary variable are missing, incomplete or not evaluable because of poor quality
The quality management detects differences in the data sets compared to source data that can´t be settled.
Presece of contra-indication for ventilation
Missing or cancelled informed consent
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Acquisition of efficacy/ clinical benefit of LUISA during primary therapy setting or switch from a clinical/ previously used home ventilator to LUISA; evaluation of efficacy/ clinical benefit by physician based on symptomatology, blood gases and patient´s acceptance
- Secondary Outcome Measures
Name Time Method