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
This trial does not accept healthy volunteersQualifiers
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 population
COPD patients with chronic hypercapnic respiratory failure needing chronic NIV will be included
Trial design
Cohort
Prospective
Treatments tested in this trial
Non-invasive ventilation
DeviceNIV as in standard care
Treatment groups
Trial outcomes
Primary outcomes
Gas exchange
Transcutaneous monitoring of gas exchange
Gas exchange
Transcutaneous monitoring of gas exchange
Gas exchange
Transcutaneous monitoring of gas exchange
Gas exchange
Transcutaneous monitoring of gas exchange
Sponsors and contacts
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University Medical Center Groningen
Lead sponsor
University of Twente
Collaborator
Löwenstein BV
Collaborator
Vivisol
Collaborator
Sencure BV
Collaborator