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