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Efficacy and Safety of Video-Imaging Single-Lumen Tracheal Tubes Combined with a Bronchial Blocker in Video-Assisted Thoracic Surgery: A Prospective Single-Arm Study

Efficacy and Safety of Video-Imaging Single-Lumen Tracheal Tubes Combined with a Bronchial Blocker in Video-Assisted Thoracic Surgery: A Prospective Single-Arm Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500111316
Enrollment
Unknown
Registered
2025-10-29
Start date
2025-11-01
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

None

Interventions

Experimental group:One-lung ventilation management using a video-imaging single-lumen tracheal tube with bronchial blocker

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion Criteria: 1. Patients scheduled for elective video-assisted thoracic surgery. 2. Aged between 18 and 80 years. 3. Requiring one-lung ventilation for >30 minutes during elective surgery. 4. American Society of Anesthesiologists (ASA) physical status classification I–III. 4. Provision of written informed consent.

Exclusion criteria

Exclusion criteria: 1. History or prediction of difficult airway, including: history of head and neck malignancy or radiotherapy, known history of difficult intubation, modified Mallampati class III–IV, mouth opening 35 kg/m²). 3. Preoperative imaging suggesting subglottic anatomical abnormalities. 4. Patients with obstructive ventilatory impairment (FEV1 <50% predicted) or restrictive ventilatory impairment (FEV1 <75% predicted). 5. Previous ipsilateral thoracic surgery or pleurodesis. 6. Presence of pulmonary infection, bronchial tumor, or tracheostomy. 7. Requirement for postoperative transfer to the ICU with an indwelling tracheal tube.

Design outcomes

Primary

MeasureTime frame
The VAS score for sore throat before leaving the operating room/post-anesthesia care unit;the VAS score for sore throat at 24 hours postoperatively;the VAS score for sore throat at 48 hours postoperatively;

Secondary

MeasureTime frame
the time required to achieve lung isolation;Lung collapse score at 10 minutes after one-lung ventilation initiation;Lung collapse score at 20 minutes after one-lung ventilation initiation;Malposition Rate;Number of intubation attempts;Success rate of first-attempt intubation;Arterial partial pressure of oxygen (PaO2) at 20 minutes after one-lung ventilation initiation;Incidence of hypoxemia (SpO2 <90%) during one-lung ventilation;Airway plateau pressure at 20 minutes after one-lung ventilation initiation;Airway injury;Arterial partial pressure of carbon dioxide (PaCO2) at 20 minutes after one-lung ventilation initiation;Airway peak pressure (after suctioning) at 20 minutes after one-lung ventilation initiation;Heart rate before anesthesia induction (T0);Heart rate after anesthesia induction but before intubation (T1);Heart rate immediately after successful tube positioning (T2);Mean arterial pressure before anesthesia induction (T0);Mean arterial pressure after anesthesia induction but before intubation (T1);Mean arterial pressure immediately after successful tube positioning (T2);Presence of hoarseness before leaving the post-anesthesia care unit/operating room;Presence of hoarseness at 24 hours postoperatively;Presence of hoarseness at 48 hours postoperatively;QoR-15 score at 24 hours postoperatively;QoR-15 score at 48 hours postoperatively;QoR-15 score at 30 days postoperatively;VAS score for sore throat at 30 days postoperatively;

Countries

China

Contacts

Public ContactHan Yongzheng

Peking University Third Hospital

hanyongzheng@bjmu.edu.cn+86 152 0130 4460

Outcome results

None listed

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