Robotic-assisted Bronchoscopy Under Moderate Sedation With Propofol
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Zurich
About this trial
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
Qualifiers
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
Disqualifiers
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
Trial design
Treatments tested in this trial
- Robotic-assisted bronchoscopy under propofol
Treatment groups
30 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov