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Terminated NCT07006311

Robotic-assisted Bronchoscopy Under Moderate Sedation With Propofol

Conditions: Lung Lesions, Robotic Assisted Bronchoscopy, Propofol, Bronchoscopy, Bronchoscopy Biopsy

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 10
Sponsor: University of Zurich

Location: University Hospital Zurich Zurich Canton of Zurich

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

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07006311). StuddyBuddy aggregates publicly available trial information.