Robotic lung biopsies without full anesthesia? small study tests feasibility
NCT ID NCT07006311
First seen Jun 26, 2026 · Last updated Jul 24, 2026 · Updated 1 time
Summary
This pilot study at the University of Zurich is testing whether robotic-assisted bronchoscopy can be performed under moderate sedation with propofol, rather than general anesthesia. Currently, robotic bronchoscopy requires full anesthesia, but standard bronchoscopy often uses lighter sedation. The study will enroll 30 adults scheduled for bronchoscopy to see if the robotic approach works safely and effectively under propofol. It is an early feasibility test, not a treatment study.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- propofol
- What this could lead to
- If successful, this could make robotic bronchoscopy more widely available by avoiding the need for general anesthesia.
- What could go wrong
- This is a very small pilot study (30 people) testing feasibility only. It may not work as well as hoped, and larger studies are needed.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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10 people
The number who actually took part.
- Started
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Aug 2025
- Finished
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Jun 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University Hospital Zurich
Zurich, Canton of Zurich, 8091, Switzerland
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