Idiopathic Pulmonary Fibrosis Clinical Trial
Official title:
Effects of an Oxymizer® During Daytime in Patients With Pulmonary Fibrosis (IPF)
This study will investigate the effects of a reservoir nasal cannula (Oxymizer®) compared to a conventional nasal cannula (CNC) in patients with idiopathic pulmonary fibrosis.
Patients will be recruited during a 3-week inpatient pulmonary rehabilitation program. They
will perform the following three interventions on consecutive days and will repeat them
after a week. During these days the time table for prescribed physical activities and
therapies will be kept in a comparable fashion.
The following 3 interventions will be performed in randomized order:
Day A: The Patient wears a conventional nasal cannula for 12 h with oxygen flow rate as
prescribed during ADL
Day B: The Patient wears the Oxymizer® with prescribed oxygen flow rate for 12 h during ADL
Day C: The patient wears the Oxymizer® with a flow rate reduced by 1l/min in comparison to
the prescribed oxygen flow rate, for 12h
The following week the same measurements will be repeated. The mean of the corresponding two
measures will be calculated for each approach.
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Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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