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Recruiting NCT07006311

Robotic-assisted Bronchoscopy Under Moderate Sedation With Propofol

Trial Parameters

Condition Lung Lesions
Sponsor University of Zurich
Study Type INTERVENTIONAL
Phase N/A
Enrollment 30
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2025-08-14
Completion 2026-06-01
Interventions
Robotic-assisted bronchoscopy under propofol

Brief Summary

In this study, the investigators want to find out whether robot-assisted bronchoscopy also works with moderate sedation (Propofol), as is already used in standard bronchoscopies. The study is being conducted as a pilot study. This means that it is an initial test run for a scientific investigation. The investigators are testing on a small scale whether the intervention works as predicted before a larger study is conducted.

Eligibility Criteria

Inclusion Criteria: * informed consent signed by the subject * aged at least 18 years * scheduled for bronchoscopy with moderate sedation and tracheal intubation in order to obtain at least 1 specimens of the lung via transbronchial biopsy * necessary periinterventional laboratory examinations needed for the bronchoscopy * judgement of the subject Exclusion Criteria: * endobronchial lesion causing lobar atelectasis * inability or contraindications to undergo bronchoscopy (e.g. severe cardiopulmonary diseases, coagulation disorders, intolerance to anesthesia or endoscopic operation, psychiatric disorders or severe neurosis) * pregnant or lactating women

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