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Comparative Clinical Study of Laryngeal Mask Airway General Anesthesia versus Double-Lumen Endotracheal Tube General Anesthesia in Thoracoscopic Lung Resection Surgery

Comparative Clinical Study of Laryngeal Mask Airway General Anesthesia versus Double-Lumen Endotracheal Tube General Anesthesia in Thoracoscopic Lung Resection Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114462
Enrollment
Unknown
Registered
2025-12-12
Start date
2025-12-15
Completion date
Unknown
Last updated
2025-12-15

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

Conditions

pulmonary nodule

Interventions

Laryngeal mask group:The procedure was performed by the same anesthesiologist proficient in both laryngeal mask airway and double-lumen endotracheal tube insertion techniques. The laryngeal mask airwa
Double-lumen Tracheal Tube Group:The procedure was performed by the same anesthesiologist proficient in both laryngeal mask airway and double-lumen endotracheal tube insertion techniques. The double-l

Sponsors

Guangyuan First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1 The patient is in good mental status with unimpaired communication, has provided informed consent, is aged 18–75 years, and gender is not restricted. 2 American Society of Anesthesiologists (ASA) physical status classification I–III, body mass index (BMI) 18–30 kg/m². 3 No history of allergy to anesthetic agents. 4 Scheduled for non-complex thoracoscopic surgery, including bullae resection, wedge resection, or lobectomy (see exclusion criteria for details). 5 Operative duration >1 hour and <=4 hours.

Exclusion criteria

Exclusion criteria: 1 Refusal to participate in this study. 2 Pre-existing coagulation disorders, hypoxemia, hypercapnia, or severe hemoptysis. 3 Acute pulmonary infection or active pulmonary tuberculosis. 4 Excessive airway secretions, high risk of aspiration/reflux, or severe pharyngeal pathology (edema, hematoma, hemorrhage, abscess, tumor). 5 Difficult airway, existing airway obstruction, or intraoperative conditions that would impede immediate endotracheal intubation. 6 Spinal deformity or cerebral edema. 7 Phrenic nerve paralysis. 8 New York Heart Association (NYHA) functional class III or IV. 9 Patient refusal or contraindications to regional nerve blockade. 10 Preoperative chest CT indicating extensive pleural adhesions, or moderate to massive pleural effusion. 11 Surgical procedure involving vascular reconstruction. 12 Other conditions deemed by the investigator to make the patient unsuitable for trial participation.

Design outcomes

Primary

MeasureTime frame
SpO2 nadir;EtCO2 peak;

Secondary

MeasureTime frame
Hemodynamic parameters;Blood Gas Analysis;Lung collapse adequacy;Incidence of Postoperative Pulmonary Complications (PPCs);Lung collapse time;Overall surgeon satisfaction;Incidence of other perioperative adverse reactions;Total anesthesia cost;

Countries

China

Contacts

Public ContactLi Zhang

Guangyuan First People's Hospital

18781229899@163.com+86 187 8122 9899

Outcome results

None listed

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