Comparison of the Oxymask and Oxy2mask on Supplemental Oxygen Delivery

Withdrawn before enrolling · Not applicable

Conditions studied: Hypoxia

In brief

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.

Key facts

Study ID

NCT06433934

Run by

Northwestern Medicine

People needed

0

Starts

2024-06-30

Expected to finish

2024-11-30

Last updated by the study team

2026-04-15

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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.

You may not qualify if…

• 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

Where it is running

• Central DuPage Hospital — Winfield, Illinois, United States

Full record on ClinicalTrials.gov

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