← Back to all trials
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
Source: ClinicalTrials.gov (NCT07006311). StuddyBuddy aggregates publicly available trial information.