Comparison of the Oxymask and Oxy2mask on Supplemental Oxygen Delivery (NCT06433934) | Clinical Trial Compass
WithdrawnNot Applicable
Comparison of the Oxymask and Oxy2mask on Supplemental Oxygen Delivery
Stopped: The PI is no longer with the institution.
United States0Started 2024-06-30
Plain-language summary
The purpose of this study is to determine if the performance of a newly released oxygen mask is the same, better, or worse than previous mask version. We will measure the flow rate necessary to maintain the same oxygen saturation in adult patients using each mask.
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* Participants have oxygen device and are being titrated per NM CDH oxygen protocol (maintained between 90%-96%; or 88% - 92% if CO2 retainer)
* Participants to have period of stability; 2 hours at same liter flow on open design mask, 5-15 lpm 02.
* All adult patients (\> 18 years old) in med surge units (bed tower)
* Post-op patients requiring oxygen on Post-op Day 2.
* Patients currently on \>5 LPM via nasal cannula, clinician can recommend the change to OxyMask. If remains on \>5 LPM via OxyMask, patient can be included.
* Oxygen protocol will be followed per standards of care.
Exclusion Criteria:
* Patients receiving home oxygen therapy who do not require additional oxygen during hospital stay.
* Patients with a history of Bleomycin therapy.
* Patients with a history of Paraquat poisoning
* Patients that are pregnant