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NCT07850856Not yet recruiting

HFNC During Bronchoscopy in COPD Patients

Clinical Study of High-Flow Nasal Cannula Oxygen Support During Bronchoscopy in COPD Patients

Source: ClinicalTrials.gov · Last updated 30 Sept 2026

Brief summary (registry, in English)

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.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
1000 (estimated)
First submitted
22 Aug 2026
Start date
1 Sept 2026
Primary completion date
31 Dec 2028
Lead sponsor
The First Affiliated Hospital of Guangzhou Medical University
Diseases
COPD
NCT number
NCT07850856

What you commit to

  • Study type: Interventional
  • Planned participants: 1000
  • From 1 Sept 2026 to the primary completion date, 31 Dec 2028
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Contraindications to bronchoscopy or anesthesia, Nosebleeds

Who the study is looking for

  • COPD ,(ASA)Ⅰ ~ Ⅲ

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.