Skip to content

Evaluation of Oxygen Delivery Through Nasal Cannula in Volunteers

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02886312
Enrollment
30
Registered
2016-09-01
Start date
2015-08-31
Completion date
2016-08-31
Last updated
2025-01-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Oxygen Delivery, Patient Comfort, Patient Monitoring

Brief summary

This study will evaluate patient comfort and oxygen delivery efficiency when providing supplemental oxygen through a nasal cannula to volunteers using an instrumented oxygen delivery system. The goals of the study are to evaluate different oxygen flow rates and oxygen delivery modes. In addition, the investigators will investigate if the system can detect apnea (cessation of breathing) and removal of the nasal cannula. The investigators will also investigate how well high flow oxygen delivered only during inspiration is tolerated and how much the end-tidal oxygen increases after two minutes of high oxygen flow delivered only during the inhalation phase of the breath.

Interventions

DEVICESupplemental Oxygen Delivery System

Sponsors

University of Utah
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Healthy volunteers drawn from the general public and students, staff, and faculty of the University of Utah.

Exclusion criteria

* Volunteers who self report respiratory diseases such as acute respiratory distress syndrome, pneumonia and lung cancer will be excluded. In addition, volunteers who self report respiratory conditions such as nasal or bronchial congestion due to a cold or allergies will be excluded.

Design outcomes

Primary

MeasureTime frameDescription
End-tidal OxygenContinuously throughout 30 minute volunteer studyDid the novel system increase end-tidal oxygen?
Patient ComfortEvery 2 minutes up to 30 minutesDid the patients feel it was more comfortable for a given end-tidal oxygen level?
End-tidal Carbon DioxideContinuously throughout 30 minute volunteer studyWas end-tidal carbon dioxide measured more accurately using the novel system?
Respiratory RateContinuously throughout 30 minute volunteer studyCompared respiratory rate against capnometry.
Oxygen SaturationContinuously throughout 30 minute volunteer studyDid the novel system increase oxygen saturation?

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026