About this trial
The aim of the data collection is to create an advanced reliable method to remotely monitor patient on chronic home non-invasive ventilation (NIV), both regarding ventilatory efficacy and patient comfort, both in the hospital and at home by assessing gas exchange, lung mechanics and the interaction between the patient and the ventilator.
For this purpose, we will set-up of databank of synchronously acquired datasets of already standard care monitored parameters during NIV (transcutaneous monitoring of gas exchange; ventilator data including data on PVA), and newly non-invasively acquired data on patient effort (EMG, patient ratings) and lung (hyper)inflation (EIT), during the set-up and follow-up of standard care chronic NIV.
Eligibility criteria
Qualifiers
COPD patients indicated for chronic home NIV
Disqualifiers
not able to read the written information and/or sign the informed consent form
no possibility to perfrom measurements at home
Trial design
Treatments tested in this trial
- Non-invasive ventilation
Treatment groups
Sponsors and collaborators
University Medical Center Groningen
Lead sponsor
University of Twente
Collaborator
Löwenstein BV
Collaborator
Vivisol
Collaborator
Sencure BV
Collaborator