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Incidence of laryngeal mask combined with visual bronchial blocker in throat injury after pneumonectomy

Incidence of laryngeal mask combined with visual bronchial blocker in throat injury after pneumonectomy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098874
Enrollment
Unknown
Registered
2025-03-14
Start date
2025-01-14
Completion date
Unknown
Last updated
2025-03-17

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

Conditions

lung cancer

Interventions

double-lumen endotracheal tube group:lung isolation with double-lumen endotracheal tube
visual bronchial blocker group:lung isolation with visual bronchial blocker

Sponsors

Shanghai Chest Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. age > 18 years old; 2. lung resection surgery; 3. ASA : I-III; 4. BMI: 18.5-30kg/m^2; 5. sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. difficult airway; 2. Patients with gastroesophageal reflux or gastric retention; 3. Patients with lung infection or bleeding; 4. Patients with severe hypofunction of the lungs; 5. Previous history of lung surgery or bilateral lung surgery; 6. Cognitive decline effects on outcome assessors; 7. Chronic sore throat or abnormal pronunciation within 24 hours before surgery; 8. abnormal bronchial opening in the right upper lung; 9. Other anesthesiologists or surgeons who are considered unsuitable for enrollment.

Design outcomes

Primary

MeasureTime frame
incidence of throat injury in 24 hours after surgery;

Secondary

MeasureTime frame
incidence of throat injury in 1 hour after surgery;incidence of throat injury in 48 hours after surgery;length of stay;hypoxemia during surgery;intubation time;hymodynamic status during intubation;the dispalcement of lung isolation tools;

Countries

China

Contacts

Public ContactWu Jingxiang

Shanghai Chest Hospital

wjx1132@163.com+86 189 3085 7186

Outcome results

None listed

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