Robotic-assisted Bronchoscopy Under Moderate Sedation With Propofol

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-08-14

Study Completion Date

2026-06-01

Brief Summary

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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.

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Detailed Description

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Conditions

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Lung Lesions Robotic Assisted Bronchoscopy Propofol Bronchoscopy Bronchoscopy Biopsy

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Pilot study

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Robotic-assisted bronchoscopy with Propofol

Group Type EXPERIMENTAL

Robotic-assisted bronchoscopy under propofol

Intervention Type DEVICE

In this study, patients will undergo a robotic-assisted bronchoscopy under moderate sedation with propofol. While the use of propofol as a sedative is common for manual bronchoscopies, robotic-assisted bronchoscopy is only permitted under general anesthesia. In the study intervention, the investigators want to test the feasibility of the combination of robotic-assisted bronchoscopy under propofol.

Interventions

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Robotic-assisted bronchoscopy under propofol

In this study, patients will undergo a robotic-assisted bronchoscopy under moderate sedation with propofol. While the use of propofol as a sedative is common for manual bronchoscopies, robotic-assisted bronchoscopy is only permitted under general anesthesia. In the study intervention, the investigators want to test the feasibility of the combination of robotic-assisted bronchoscopy under propofol.

Intervention Type DEVICE

Eligibility Criteria

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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

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No