Working title: Change in intrathoracic gas volume after noninvasive ventilation in patients with suspected deventilation syndrome.
- Conditions
- J44.9J96.19Chronic obstructive pulmonary disease, unspecified
- Registration Number
- DRKS00027953
- Lead Sponsor
- Kliniken der Stadt Köln gGmbH, Lungenklinik Standort-Merheim
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Patients with pre-existing and newly diagnosed COPD of any stage according to GOLD with established home NIV therapy.
Deventilation syndrome defined as morning dyspnea symptoms after cessation of NIV therapy
Consent to privacy policy and patient education.
Verbal and cognitive ability to respond to questionnaires
Exclusion Criteria
Patient age <18 years
Alexia, deafness
Patients not capable of giving consent
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary endpoint is the comparison of bodyplethysmographic and respiratory muscular parameters before and after four hours of NIV use.
- Secondary Outcome Measures
Name Time Method Secondary endpoints are the comparison of the evaluation of the data from the patient catalog, as well as the SRI questionnaire and the ventilator settings and device data.