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The Effects of High-flow Nasal Oxygen on Oxygenation During Rigid Bronchoscopy Under General Anesthesia in Pediatric Patients

The Effects of High-flow Nasal Oxygen on Oxygenation During Rigid Bronchoscopy Under General Anesthesia in Pediatric Patients: A Prospective Observational Pilot Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03905733
Enrollment
20
Registered
2019-04-05
Start date
2019-04-30
Completion date
2021-04-30
Last updated
2019-04-05

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

Conditions

Foreign Bodies, Tumor, Stenosis of Trachea, Bronchus

Brief summary

The aim of this study is to evaluate the effect of high-flow nasal cannula oxygen administration on maintenance of oxygenation and removal of carbon dioxide during apnoeic period in pediatric patients undergoing general anesthesia with rigid bronchoscopy

Interventions

DEVICEOptiflow

supply of oxygen at 2 L / min/ kg through Optiflow

Sponsors

Yonsei University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 7 Years
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 7 or younger who meet American Society of Anesthesiologists (ASA) physical class 2-4

Exclusion criteria

* 1\. Patients undergoing extracorporeal membrane oxygenation (ECMO) * 2\. Patients with active nasal bleeding), severe nasal obstruction, recent nasal trauma of surgery * 3\. Patients with current maxillofacial trauma or basal skull fracture * 4\. Patients with active nasal bleeding), severe nasal obstruction, recent nasal trauma of surgery * 5\. Extremely low birth weight infant and premature infant less than 28 weeks gestation age * 6\. Patients who had previously undergone rigid bronchoscopy / surgery * 7\. If the parent of subject includes a person who can not read the written consent (eg, illiterate, foreigner, etc.)

Design outcomes

Primary

MeasureTime frameDescription
Hypoxia occurs the first timeThe time taken to reach the point at which peripheral oxygen saturation fell below 90% for the first time immediately after the onset of apnea intraoperatively.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
the lowest oxygen saturationapnea period during the rigidbroscopic procedure/surgerythe lowest value of oxygen saturation measured percutaneously at extremity.
Occurence of hypoxic eventapnea period during the rigidbroscopic procedure/surgeryOccurence of hypoxic event: Presence or absence of hypoxia(peripheral oxygen saturation fell below 90% ) during rigid bronchoscopy

Secondary

MeasureTime frame
End-tidal carbon dioxide partial pressureend-tidal CO2 partial pressure after 3 consecutive breaths after intubation or insertion of laryngeal mask following end of apnea during intraoperative period.
Arterial oxygen / carbon dioxide partial pressureshortly before start of apnea (within 30 seconds) and shortly after end of apnea (within 30 seconds)

Countries

South Korea

Outcome results

None listed

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