Helmet CPAP Versus HFNC in COVID-19
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- STATUS
- Recruiting
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- participants needed
- 120
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- sponsor
- Lund University
Summary
We aim to investigate whether the use of Continuous Positive Airway Pressure using a Helmet device (Helmet CPAP) will increase the number of days alive and free of ventilator within 28 days compared to the use of a High Flow Nasal Cannula (HFNC) in patients admitted to Helsingborg Hospital, Sweden, suffering from COVID-19 and an acute hypoxic respiratory failure.
Description
A detailed description can be found in the study protocol which is pending submission for peer-review.
Details
Condition | COVID, Acute Hypoxemic Respiratory Failure |
---|---|
Age | 18years - 100years |
Treatment | HFNC, Helmet CPAP |
Clinical Study Identifier | NCT04395807 |
Sponsor | Lund University |
Last Modified on | 16 February 2024 |
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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