Oxygen delivery devices in bronchoscopy procedures and the effect on oxygenatio

Not Applicable

Recruiting

• Conditions: Hypoxia/desaturations during bronchoscopy; Comfort of oxygen delivery devices during bronchoscopy procedures; Respiratory - Other respiratory disorders / diseases

• Registration Number: ACTRN12623001262695
• Lead Sponsor: Georgia Burton

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-12-05
• Last Update Posted: 10 June 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 120

Inclusion Criteria

• Age 18 years or older
• Indication for diagnostic bronchoscopy (standard bronchoscopy or EBUS guided)
• Pre-procedure intent to insert bronchoscope via the nose in the standard bronchoscopy group (stratum one)

Exclusion Criteria

• Not able to consent
• Patient is in ICU
• Patient is in theatre
• Patient is intubated
• Patient has a tracheostomy
• Pre-procedure intent to insert bronchoscope via the mouth in the standard bronchoscopy group (stratum one)

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Time with SpO2 <90% during bronchoscopy [Time in seconds measured with Nox T3s device (Noxturnal, Iceland) At any point during bronchoscopy - from the point that the monitoring device is attached to the point at which it is removed. Continuous SpO2 monitoring throughout procedure.]