HFNC During Bronchoscopy in COPD Patients
HFNC COPD
Clinical Study of High-Flow Nasal Cannula Oxygen Support During Bronchoscopy in COPD Patients
1 other identifier
interventional
1,000
0 countries
N/A
Brief Summary
Bronchoscopy diagnosis and treatment is highly irritating, and the effect of local topical anesthesia is poor; the airway is shared; and COPD patients have low oxygen reserves due to impaired lung function. At present, clinical anesthesia generally uses nasal cannula for oxygen inhalation. If the anesthesia is too shallow, it may cause airway spasm, and if the anesthesia is too deep, it will inhibit breathing and lead to hypoxia. Hypoxemia has been reported in 66% of COPD patients undergoing sedation for bronchoscopy. Therefore, solving hypoxia is the biggest problem in anesthesia for bronchoscopy diagnosis and treatment.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Sep 2026
Longer than P75 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 22, 2026
CompletedStudy Start
First participant enrolled
September 1, 2026
CompletedFirst Posted
Study publicly available on registry
September 30, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2030
September 30, 2026
September 1, 2026
2.3 years
August 22, 2026
September 27, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
pulse oximetry
Blood oxygen saturation during anesthesia, record the duration and number of times below 90%
The entire anesthesia period during bronchoscopy
Study Arms (2)
Group N
OTHERGroup N used traditional nasal cannula to inhale oxygen during anesthesia.
Group HFNC
EXPERIMENTALDuring anesthesia, the HFNC group used nasal high-flow oxygen inhalation
Interventions
1000 COPD patients who underwent bronchoscopy were randomly divided into 2 groups in a 1:1 ratio.Nasal high-flow oxygen therapy group(group N) and nasal cannula oxygen inhalation group(group HFNC).The N group used traditional nasal cannula for oxygen inhalation, and the HFNC group used nasal high-flow oxygen inhalation.
1000 COPD patients who underwent bronchoscopy were randomly divided into 2 groups in a 1:1 ratio.Nasal high-flow oxygen therapy group(group N) and nasal cannula oxygen inhalation group(group HFNC).The N group used traditional nasal cannula for oxygen inhalation, and the HFNC group used nasal high-flow oxygen inhalation.
Eligibility Criteria
You may qualify if:
- COPD ,(ASA)Ⅰ ~ Ⅲ
You may not qualify if:
- Contraindications to bronchoscopy or anesthesia, Nosebleeds
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Masking Details
- Open Label
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- deputy chief physician
Study Record Dates
First Submitted
August 22, 2026
First Posted
September 30, 2026
Study Start
September 1, 2026
Primary Completion (Estimated)
December 31, 2028
Study Completion (Estimated)
December 31, 2030
Last Updated
September 30, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will share
- Time Frame
- Beginning 6 months and ending 5 years following publication of primary results.
- Access Criteria
- Researchers who provide a methodologically sound proposal. Proposals should be directed to \[your email\]. To gain access, data requestors will need to sign a data access agreement.
Upon completion of the study, de-identified individual participant data (IPD) and relevant supporting documents (e.g., study protocol, statistical analysis plan) will be shared upon reasonable request with researchers who provide a methodologically sound research proposal. Data will be made available starting 6 months after publication of the primary results and will remain available for 5 years. Requests must be submitted via \[designated email or website\], and a data use agreement must be signed.