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Nasal High Flow (NHF) Therapy Use Following Hospitalization for an Exacerbation of COPD: A Feasibility Study
The aim of this feasibility study is to provide data for a subsequent randomized controlled trial to investigate if patient outcomes will be improved after an acute COPD exacerbation using domiciliary nasal high flow therapy (NHF) compared to standard care. This feasibility study will investigate the following: process, resources, management and scientific aspects of delivering NHF as an adjunct therapy in COPD patients.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Alana HealthCare
Liverpool, New York, United States
Medical Research Institute of New Zealand
Wellington, New Zealand
Start Date
November 1, 2015
Primary Completion Date
May 3, 2017
Completion Date
May 3, 2017
Last Updated
August 17, 2020
29
ACTUAL participants
NHF with or without Oxygen
DEVICE
Lead Sponsor
Fisher and Paykel Healthcare
Collaborators
NCT07477600
NCT07462221
NCT05878769
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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