NCT07467005Not yet recruiting
Video Double-Lumen Tube for Secondary Pulmonary Resection
Video Double-Lumen Tube for Secondary Pulmonary Resection: A Multicenter Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 12 Mar 2026
Brief summary (registry, in English)
During thoracic surgery, double-lumen endotracheal intubation with one-lung ventilation is routinely performed to optimize surgical exposure, facilitate operative manipulation, and prevent iatrogenic lung injury. In patients undergoing repeat pulmonary surgery, prior lung resection may lead to pleural adhesions and tracheobronchial distortion, which substantially increase the difficulty of bronchial intubation. Even with experienced operators, the malposition rate of conventional double-lumen tubes remains high. The video double-lumen tube enables continuous visualization of the trachea and carina during insertion, positioning, and one-lung ventilation, allowing real-time airway monitoring. However, no clinical studies have specifically investigated airway management in patients undergoing redo pulmonary surgery. This study aimed to evaluate the efficacy and safety of the video double-lumen tube during anesthesia in patients undergoing secondary pulmonary resection.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 500 (estimated)
- First submitted
- 9 Mar 2026
- Start date
- 16 Mar 2026
- Primary completion date
- 1 Dec 2027
- Lead sponsor
- Zhejiang University
- Diseases
- Lung cancer
- NCT number
- NCT07467005
What you commit to
- Study type: Interventional
- Planned participants: 500
- From 16 Mar 2026 to the primary completion date, 1 Dec 2027
- 3 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Acute respiratory distress syndrome (ARDS) or respiratory failure within the past 3 months.
- Other conditions deemed unsuitable by the investigator.
Other
- Preoperatively predicted difficult airway (Mallampati ≥ III, Cormack-Lehane ≥ III).
- Uncontrolled asthma.
- Confirmed pregnancy or current breastfeeding.
- Multiple traumatic injuries.
- Current participation in another clinical trial.
Who the study is looking for
- Age ≥18 years.
- History of previous pulmonary resection.
- Scheduled for elective pulmonary surgery.
- Planned to receive a left-sided double-lumen tube.
- ASA physical status I-III.
- Patients have signed the informed consent form.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (3)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Zhejiang Cancer Hospital Coordinator of this site? Confirm its status | Hangzhou | China | Unknown status |
| The First Affiliated Hospital Zhejiang University School of Medicine Coordinator of this site? Confirm its status | Hangzhou | China | Unknown status |
| The Fourth Affiliated Hospital, Zhejiang University School of Medicine Coordinator of this site? Confirm its status | Yiwu | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.