Lung nodule biopsy showdown: which method wins?
NCT ID NCT04250194
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at 288 people with a lung nodule to see which biopsy method works better: CT-guided biopsy (needle through the chest wall) or navigation bronchoscopy (a tube through the airways). The goal was to find which approach gives a clear diagnosis with fewer side effects. Results will help guide doctors in choosing the safest and most accurate procedure.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could help doctors choose the best biopsy method for lung nodules, improving diagnosis and reducing complications.
- What could go wrong
- This is a completed study comparing existing procedures, not testing a new treatment. Results may not apply to all patients or settings.
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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288 people
The number who actually took part.
- Started
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May 2020
- Finished
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Jul 2024
- 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: * Patient is referred for biopsy of a single indeterminate pulmonary nodule, with the following characteristics regarding size, location, accessibility, and probability of malignancy: * Intermediate pre-test probability of malignancy as defined by a pre-test probability of malignancy between 10% and 100%, using a validated clinical prediction model, which is either: * The Brock model14 if no PET scan data are available, or * The Herder model15 if PET-CT data are available. * Size between 10 and 30 mm (long diameter). * Location peripheral, here defined as occupying the middle or outer third lung zones. * Accessible via navigation bronchoscopy and also accessible via CT-guided biopsy (i.e. the nodule is clinically suited to equal access by either procedure), as confirmed by an independent interventional panel. Exclusion Criteria: * Patients with proximal nodules, as defined by nodules present in the proximal 1/3 of the lung by dedicated software analysis (described below) will not be eligible for the study. * Patients with multiple nodules requiring biopsy (patients may have other nodules not considered for biopsy).
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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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Duke University Medical Center
Durham, North Carolina, 27710, United States
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Kootenai Health
Coeur d'Alene, Idaho, 83814, United States
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Medical College of Wisconsin
Milwaukee, Wisconsin, 53226, United States
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Rush University Medical Center
Chicago, Illinois, 60612, United States
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Saint Luke's Hospital of Kansas City
Kansas City, Missouri, 64111, United States
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University of California, San Diego
San Diego, California, 92037, United States
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Vanderbilt-Ingram Cancer Center
Nashville, Tennessee, 37232, United States
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