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NCT07117539: PLIAP

Impact of Different Lung Isolation Devices on Pharyngolaryngeal Injuries After Pulmonary Resection

Completed NA Last updated 15 January 2026
What this trial tests

NA trial testing visual bronchial blocker (VBB) in Pulmonary Neoplasm in 270 participants. Completed in 30 November 2025.

Timeline
18 August 2025
Primary endpoint
31 October 2025
30 November 2025

Quick facts

Lead sponsorTingting Li
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeother
Enrollment270
Start date18 August 2025
Primary completion31 October 2025
Estimated completion30 November 2025
Sites3 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Tingting Li

Who can join

18 and older, any sex, with Pulmonary Neoplasm. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this clinical trial is to assess the impact of laryngeal mask combined with visual bronchial blocker on pharyngolaryngeal injury after pulmonary resection in patients with pulmonary nodules. The main question it aims to answer is: the incidence of postoperative pharyngolaryngeal injury within 24h : sore throat and hoarseness ? Researchers will compare the visual bronchial blocker group (VBB) with the double-lumen endotracheal tube group (DLT) to see if the visual bronchial blocker group can minimize laryngopharyngeal injury after pulmonary resection.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Laryngeal mask airway combined with visual bronchial blocker versus double-lumen tube for lung isolation in video-assisted thoracoscopic surgery: a protocol for a multicentre randomised controlled trial.
    Zhang Y, Li T, Wei J, Bao R, et al · · 2025 · PMID 41469076 · DOI 10.1136/bmjopen-2025-110539

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Other recruiting trials for Pulmonary Neoplasm

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Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07117539.

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