Viewing Study NCT02552732


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Study NCT ID: NCT02552732
Status: TERMINATED
Last Update Posted: 2020-08-17
First Post: 2015-09-15
Is NOT Gene Therapy: False
Has Adverse Events: True

Brief Title: Nasal High Flow Therapy 30 Day Readmission Study
Sponsor: Fisher and Paykel Healthcare
Organization:

Study Overview

Official Title: Nasal High Flow (NHF) Therapy Use Following Hospitalization for an Exacerbation of COPD: A Feasibility Study
Status: TERMINATED
Status Verified Date: 2020-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Study terminated due to change in business of US site.
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: N3ADS
Brief Summary: 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.
Detailed Description: None

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: