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Comparison of Lateral Decubitus and Supine Positions for Double-Lumen Endobronchial Tube Intubation in Video-Assisted Thoracoscopic Lung Cancer Resection: A Randomized Controlled Trial

Comparison of Lateral Decubitus and Supine Positions for Double-Lumen Endobronchial Tube Intubation in Video-Assisted Thoracoscopic Lung Cancer Resection: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123460
Enrollment
Unknown
Registered
2026-04-27
Start date
2026-04-27
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Lung Cancer

Interventions

Control Group(A) : supine position Group:double-lumen endobronchial tube intubation in the supine position
Experimental Group(B): left lateral position Group:double-lumen endobronchial tube intubation in the left lateral position
Experimental Group(c): right lateral position Group:double-lumen endobronchial tube intubation in the right lateral position

Sponsors

Beijing Chao-Yang Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18 to 75 years, scheduled for elective video-assisted thoracoscopic lung cancer resection surgery requiring one-lung ventilation; 2. American Society of Anesthesiologists (ASA) physical status classification I to III; 3. Requiring left-sided double-lumen endobronchial tube intubation;

Exclusion criteria

Exclusion criteria: 1. Patients with anticipated difficult tracheal intubation and/or difficult mask ventilation, such as those with thyromental distance 30 kg/m²; 2. Severe spinal deformity or restricted cervical spine mobility; 3. Severe cardiovascular disease (e.g., unstable angina, severe arrhythmia, left ventricular ejection fraction <40%); 4. Pre-existing neuromuscular disease, shoulder joint disease, or shoulder pain; 5. Emergency surgery, pregnancy, or severe cardiopulmonary dysfunction; 6. History of high risk of reflux and aspiration or airway tumors; 7. Any other condition deemed by the investigator to be inappropriate for participation in this study.

Design outcomes

Primary

MeasureTime frame
First-attempt intubation success rate;Total Intubation Time;—

Secondary

MeasureTime frame
Hemodynamic Stability;Severity of Postoperative Shoulder Pain;Surgical Positioning Preparation Time;Complications and Safety;Modified Cormack-Lehane (CL) classification;Number of Medical Staff Involved in Patient Positioning;—

Countries

China

Contacts

Public ContactYu Yang

Beijing Chao-Yang Hospital, Capital Medical University

13681162027@163.com+86 10 8523 1330

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026