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Post Market Study to Collect Data for Software Recognizing the Anatomical Structures During Bronchoscopy.

A Prospective, Multicenter, Post Market Study to Collect Data for Software Recognizing the Anatomical Structures as Well as Abnormalities in the Lung During a Bronchoscopy.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04770675
Enrollment
833
Registered
2021-02-25
Start date
2020-12-01
Completion date
2021-12-31
Last updated
2022-05-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemoptysis, Pulmonary Disease, Tumor

Keywords

bronchoscope

Brief summary

The primary aim is to develop a software algorithm that has the capacity to detect the normal 18 anatomical structures of the lung by using the position of the scope during the bronchoscopy procedure and using existing bronchoscopy technology.

Detailed description

2.000 subjects, preferable 150-200 number of patients per site. The 2.000 videos will be divided into an 80%/20% split (training and testing). It is a wish to obtain a spread of videos coming from across Europe, preferable from Germany, France and Denmark, with up to 800 videos coming from Denmark The patient population indicated are patients indicated for full airway bronchoscopy. Of this group it is the aim to enrol the following: 1. Patients with obstructing tumors (when tumor blocks the view of the camera) - no more than 5% (120 patients) of studies 2. Bronchoscopies on indication of haemoptysis (active bleeding) - no more than 5% (120 patients) of studies 3. Patients with stents or valves - no more than 5% (120 patients) of studies bronchoscopies. 4. Patients with former lung operations, partial or full resections - no more than 2% (48 patients).

Interventions

DIAGNOSTIC_TESTBronchoscopy

All subjects who are scheduled for a bronchoscopy may be eligible.

Sponsors

Ambu A/S
CollaboratorINDUSTRY
Qmed Consulting A/S
Lead SponsorINDUSTRY

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Oral and written participant information has been given (NA for Denmark) 2. The subject has signed informed consent (NA for Denmark) 3. Patients indicated for full airway bronchoscopy (identifying all 18 anatomical segments) 4. Patients older than 18

Exclusion criteria

1. Subject with serious lung disease which investigator considers not appropriate for this examination. 2. Lack of patient cooperation for bronchoscopy (patient with mental disorders, dysgnosia, psychological disorder…) 3. Subjects unable to give consent (NA for Denmark)

Design outcomes

Primary

MeasureTime frameDescription
Number of anatomical segments accessed during bronchoscopy1 dayaccurate photo documentation of all 18 anatomical segments +/- abnormalities

Secondary

MeasureTime frameDescription
Number of anatomical segments identified1 dayIdentified anatomical segments by the core lab/ Identified anatomical segments by the Machine Learning (after training, using the test videos).
Rate of total number of lesions detected1 daytotal lesions detected by the core lab/ total lesions detected by Machine Learning (after training, using the test videos).
Number of sections and lesions detected by core lab and machine learning1 dayAnatomical sections + lesions detected by core lab versus anatomical sections + lesions detected by machine learning

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026