Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
52 participants
INTERVENTIONAL
2021-01-22
2022-06-22
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Oxygen use
Patients will use standard oxygen via face mask of nasal prongs as usual care.
Standard oxygen
COT describes the application of low-flow oxygen in any way (Hudson mask, nasal prongs,...).
NHF use
Patients will use NHF instead of oxygen. Oxygen will be supplemented via the NHF flow.
Nasal high-flow
F is combination of room air supplemented with oxygen can be better patients. This gas mixture will be provided to the patient with a specialized nasal prong.
Interventions
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Standard oxygen
COT describes the application of low-flow oxygen in any way (Hudson mask, nasal prongs,...).
Nasal high-flow
F is combination of room air supplemented with oxygen can be better patients. This gas mixture will be provided to the patient with a specialized nasal prong.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* acute hyperemic or hypercapnia respiratory failure
Exclusion Criteria
* indication for NIV therapy
* influences of primary endpoint (rip fracture, lung embolism)
* tracheostomy
* other interventional trials
* noncompliance
18 Years
100 Years
ALL
No
Sponsors
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Jens Bräunlich
OTHER
Responsible Party
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Jens Bräunlich
Chair Pneumology and Respiratory Medicine
Principal Investigators
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Jens Bräunlich, MD
Role: STUDY_CHAIR
chair
Locations
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Klinikum Emden
Emden, , Germany
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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01
Identifier Type: -
Identifier Source: org_study_id
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