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Comparison of the application of double cuffs bronchial blocker and single cuff bronchial blocker in thoracoscopic lobectomy

Comparison of the application of double cuffs bronchial blocker and single cuff bronchial blocker in thoracoscopic lobectomy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086472
Enrollment
Unknown
Registered
2024-07-02
Start date
2024-07-02
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Thoracoscopic lung surgery

Interventions

Group D (double cuffs bronchial blocker):Double cuffs bronchial blocker was used during one lung ventilation
Group S (single cuffs bronchial blocker):Single cuff bronchial blocker was used during one lung ventilation

Sponsors

Nanpi people's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) 80 patients undergoing thoracoscopic lobectomy in our hospital were selected; (2) ASA grade I-II; (3) The age ranged from 18 to 65 years old, and the body mass index (BMI) ranged from 18.5 to 25 kggm2; (4) There was no significant abnormality in pulmonary function, and the one second rate (FEV1/FVC%) was>70%, with unlimited or obstructive ventilation dysfunction; (5) No obvious abnormality of cardiac function, no cardiovascular disease, ejection fraction (EF)>50%; (6) There was no anemia or other hematological diseases and no history of radiotherapy and chemotherapy before operation; (7) They agreed to participate in the study and signed the informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients or their families refuse to participate in the trial; (2) Moderate and above abnormal cardiopulmonary function; (3) History of bronchial asthma and airway hyperresponsiveness; (4) Patients with pulmonary infection, bronchopleural fistula, emphysema, pulmonary bullae; (5) The length of the right main bronchus was less than 0.5cm; (6) Patients with contraindications to the use of occluder such as tumor in the airway.

Design outcomes

Primary

MeasureTime frame
Number of BB displacement;

Secondary

MeasureTime frame
Time required for placement of BB;Classification of lung collapse;The incidence of hypoxemia;Surgeon satisfaction;Tracheal injury under bronchoscopy;The contamination rate of non-surgical lobe/s on the surgical side under fiberoptic bronchoscopy;The incidence of cardiovascular adverse events;Blood gas analysis indicators at different time points;Pulmonary complications one day after surgery;Length of hospital stay;Hospitalization expenses;

Countries

China

Contacts

Public ContactGuoliang Tang

Nanpi people's Hospital

zhouchao870607@163.com+86 189 3178 3019

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 23, 2026