Can laser guidance make lung biopsies safer and more accurate?
NCT ID NCT06741826
First seen Sep 08, 2026 · Last updated Sep 09, 2026 · Updated 1 time
Summary
This trial tests whether using a laser-based imaging tool called confocal laser endomicroscopy (pCLE) to guide lung biopsies improves diagnosis in people with suspected interstitial lung disease. Researchers will compare this approach with the standard method, which uses X-ray guidance. The study includes 430 adults whose diagnosis remains unclear after standard tests, and it measures how often the biopsy leads to a specific diagnosis and whether complications occur.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Probe-based confocal laser endomicroscopy (pCLE) guidance during transbronchial lung cryobiopsy
- What this could lead to
- If pCLE guidance improves biopsy accuracy, it could lead to more precise diagnoses of interstitial lung disease with fewer complications.
- What could go wrong
- The trial is at one center and may not reflect broader practice. pCLE adds complexity and might not improve outcomes enough to justify its use.
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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430 people
The number who actually took part.
- Started
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Dec 2025
- Finished
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Jul 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.
Eligibility Criteria: 1. adults with suspected interstitial lung disease (ILD). 2. Clinical and HRCT findings insufficient to establish a definitive diagnosis. 3. Histopathological evaluation by TBLC considered necessary after multidisciplinary discussion. 4. Age ≥18 years 5. Written informed consent provided. Exclusion Criteria: 1. Contraindications to bronchoscopy or TBLC. 2. Severe hypoxemia or uncontrolled bleeding risk. 3. Severe pulmonary hypertension or unstable cardiopulmonary disease. 4. Active infection. 5. Pregnancy. 6. Inability to provide informed consent.
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Conditions
The condition(s) this trial relates to.
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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China-Japan Friendship Hospital
Beijing, China
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