A pilot study comparing oxygen delivery from 4 different delivery devices under hyperbaric conditions on healthy volunteers.

Not Applicable

Completed

• Conditions: hypoxemia; Anaesthesiology - Other anaesthesiology

• Registration Number: ACTRN12622001545752
• Lead Sponsor: Kenneth Lo

Brief Summary

Demonstrated it is possible to measure the intra-device oxygen level under pressurised condition using an external side stream analyser outside the hyperbaric chamber. There are differences in intra-device oxygen levels, comfort, and breathability. This shows it is feasible to conduct a similar and larger study.

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2022-04-30
• Study Start: 2022-12-13
• Last Update Posted: 9 January 2023

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 6

Inclusion Criteria

The volunteers for this study were healthy non-smoking technicians and doctors of both sexes

Exclusion Criteria

any patients
any emergency treatment

Study & Design

• Study Type: Observational
• Study Design: Not specified