NCT07850856

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

65
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,000

participants targeted

Target at P75+ for not_applicable

Timeline
52mo left

Started Sep 2026

Longer than P75 for not_applicable

Status
not yet recruiting

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

Study Progress2%
Sep 2026Dec 2030

First Submitted

Initial submission to the registry

August 22, 2026

Completed
10 days until next milestone

Study Start

First participant enrolled

September 1, 2026

Completed
29 days until next milestone

First Posted

Study publicly available on registry

September 30, 2026

Completed
2.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2028

Expected
2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2030

Last Updated

September 30, 2026

Status Verified

September 1, 2026

Enrollment Period

2.3 years

First QC Date

August 22, 2026

Last Update Submit

September 27, 2026

Conditions

Keywords

HFNCCOPD

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

OTHER

Group N used traditional nasal cannula to inhale oxygen during anesthesia.

Other: group N used traditional nasal cannula for oxygen inhalation

Group HFNC

EXPERIMENTAL

During anesthesia, the HFNC group used nasal high-flow oxygen inhalation

Other: Group HFNC 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.

Group N

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.

Group HFNC

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Pulmonary Disease, Chronic Obstructive

Condition Hierarchy (Ancestors)

Lung Diseases, ObstructiveLung DiseasesRespiratory Tract DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
Open Label
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: This study compared the effects of nasal cannula oxygen inhalation and high-flow nasal oxygen therapy (HFNC) on bronchoscopy under anesthesia in COPD patients.
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

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.

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.