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Application of visual single lumen tracheal tube combined with bronchial occluder in right lung wedge resection

Application of visual single lumen tracheal tube combined with bronchial occluder in right lung wedge resection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099346
Enrollment
Unknown
Registered
2025-03-21
Start date
2025-03-30
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

Lung tumor

Interventions

Experimental group:A visual single-lumen endotracheal tube is combined with a bronchial occluder
Control group:A conventional single-lumen endotracheal tube is used in combination with a bronchial occluder

Sponsors

Department of Anesthesiology, Lishui People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: The age range of subjects who signed the informed consent form was 18 to 75 years old; American Society of Anesthesiologists (ASA) health status classification of I. to II; Elective right lung wedge resection is planned

Exclusion criteria

Exclusion criteria: 1. For patients who need to undergo negative pressure aspiration during surgery to alleviate bronchiectasis, empyema, hemothorax and other conditions; 2. Patients whose bronchial opening in the upper lobe of the right lung is higher and the opening of the right upper lung is shorter than 1.5cm from the carina; 3. Patients with lesions involving the main airway or those who need to perform major airway-related operations during surgery.

Design outcomes

Primary

MeasureTime frame
Time required for pipe plugging and sealing;

Secondary

MeasureTime frame
The number of times the occluder has been displaced;Number of times the fiberoptic scope was used intraoperatively;Time required for intubation;

Countries

China

Contacts

Public ContactRenhong He

Lishui People's Hospital

hyt88888@163.com+86 189 5709 0889

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026