Skip to content

High-flow Nasal Oxygen During Rigid Bronchoscopy Under General Anesthesia: a Randomized Controlled Trial

High-flow Nasal Oxygen During Rigid Bronchoscopy Under General Anesthesia: a Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03892408
Enrollment
56
Registered
2019-03-27
Start date
2019-04-21
Completion date
2022-08-19
Last updated
2024-06-13

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

Conditions

Bronchus Tumour, Foreign Bodies, Stenosis Trachea, Tumor

Brief summary

The aim of this study is to evaluate the effect of high-flow nasal cannula oxygen administration on apnea in patients undergoing general anesthesia with rigid bronchoscopy compared with standard anesthesia methods.

Interventions

DEVICEOptiflow ™

supply of 100 % of oxygen at 70 L / min through Optiflow ™ (Fisher and Paykel Healthcare Limited, Auckland, New Zealand) plus standard oxygen supply through rigid bronchoscope during apnea period.

Sponsors

Yonsei University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Masking description

triple (Participant, Care Provider, investigator)

Intervention model description

A prospective Randomized, open label Trial

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 1\. Patients undergoing general anesthesia with stent placement or bougination, biopsy or removal of a foreign body or a mass through a rigid bronchoscope * 2\. Patients aged 19 or older who meet American Society of Anesthesiologists (ASA) physical class 2-4

Exclusion criteria

* 1\. Patients with dementia or cognitive impairment * 2\. pregnant women * 3\. Patients undergoing extracorporeal membrane oxygenation (ECMO) * 4\. Patients with active nasal bleeding), severe nasal obstruction, recent nasal trauma of surgery * 5\. Patients with current maxillofacial trauma or basal skull fracture * 6\. Patients who had previously undergone rigid bronchoscopy / surgery * 7\. If the subject includes a person who can not read the written consent (eg, illiterate, foreigner, etc.)

Design outcomes

Primary

MeasureTime frameDescription
the lowest oxygen saturationapnea period during the rigidbroscopic procedure/surgerythe lowest value of oxygen saturation measured percutaneously at extremity.

Secondary

MeasureTime frame
Hypoxia occurs the first timeintraoperative (The time taken to reach the point at which peripheral oxygen saturation fell below 90 for the first time immediately after the onset of apnea)
End-tidal carbon dioxide partial pressureIntraoperative (end-tidal CO2 partial pressure after 3 consecutive breaths after intubation or insertion of laryngeal mask following end of apnea)
Arterial oxygen / carbon dioxide partial pressureshortly before start of apnea (within 30 seconds)
hypoxemia related surgical interruptions4) hypoxemia related surgical interruptions during apneic period

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026