None listed
Conditions
Interventions
Control:Ordinary occluder
Experimental group:Visual occluder
Sponsors
The First People’s Hospital of Lianyungang
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Aged > 18 years, gender not limited; 2. Body Mass Index (BMI) < 30 kg/m2; 3. ASA grades I to III; 4. Patients undergoing lung resection with pulmonary isolation using a sealing tube; 5. Voluntarily participated and signed the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Patients with bronchiectasis, empyema, hemothorax, etc. who require convenient negative pressure suction during the operation; 2. CT examination shows: The opening of the bronchus in the upper lobe of the right lung is relatively high, located above the carina. This is observed in the patient. 3. Patients whose lesions involve the main airway or for whom main airway procedures need to be performed during the operation; 4. Weight lower than or higher than the standard weight by 15%; 5. Participated in other drug trials within the past three months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The success rate of one-time intubation; | — |
Secondary
| Measure | Time frame |
|---|---|
| Intraoperative and postoperative adverse reactions;Rate of tube displacement during occlusion;Intubation time (The time when the laryngoscope is inserted into the tracheal tube to the appropriate depth);Placement and positioning time of the blocker in supine position (from picking up the blocker tube to positioning completion).; | — |
Countries
China
Contacts
Public ContactWu Yong
The First People’s Hospital of Lianyungang
Outcome results
None listed