No registrations found.
ID
Source
Brief title
Health condition
COPD and pneumonia
Sponsors and support
Intervention
Outcome measures
Primary outcome
Primaire parameter is comfort. we ask patients to complete CCQ daily during admittion
Secondary outcome
Besides the primaire parameter, there will also measurements to investigate cough, dyspnea, oxygenation, respiration, heartfrequency, viscocity of the mucus and duration of admittion
Background summary
Patients admitted on the lungward have different lungproblems, with oxgenation problems as the result. This is treated with oxygen therapy. There are several methods of administration oxygen. Most commonly used is a tube under the nostrils applying oxygen. The Nasal high flow is also used for a numbre of years now, but only with patients with higher oxygen needs. This application has multiple benefits. Eg: heated and humidified oxygen and a higher flow. The aim of this study is to determine if the use of Nasal high flow in patients with exacerbation COPD and/of pneumonia gives more comfort and a faster recovery then regular oxygen therapy. This is a randomized intervention study. Patients are randomized into 2 groups. Patients in the intervention group receive oxygen therapy by the nasal high flow. The control group receive oxygen by the regular oxygen application.
Study objective
The aim of this study is to determine if the use of Nasal high flow in patients with exacerbation COPD and/of pneumonia gives more comfort and a faster recovery then regular oxygen therapy.
Study design
First inclusion is planning 1 week of decembre
Intervention
Patients will be randomized into 2 groups: the standard care group will receive oxygen therapy by the regular oxygen application. The intervention group will receive oxygen by the Nasal high flow.
Inclusion criteria
Exacerbation COPD and/or pneumonia using a minimal of 1 liter oxygen/minute
Exclusion criteria
- Indication voor NPPV
- Pneumothorax
- Delirium
- ILD patients
- Patients post lungtransplantation
- Astma patients without persisting obstruction
- Patient using Bi-pap or C-pap at home
- Patients who are not able to read and speak Dutch
Design
Recruitment
IPD sharing statement
Plan description
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL8196 |
Other | MEC-U : R19.053 |