Robot-Guided dye injection could make lung nodule surgery more precise
NCT ID NCT07177924
First seen Jun 25, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This study tests a robotic bronchoscope to inject a dye near small lung nodules before they are removed surgically. The dye helps surgeons see the nodule during operation, making removal more accurate. Fifty patients with hard-to-find nodules will be enrolled, and researchers will measure how often the dye is placed correctly and how well the surgery goes. The goal is to improve success rates and reduce complications.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Indocyanine green (ICG) dye mixed with iodinated contrast
- What this could lead to
- If successful, this technique could make lung nodule removal more precise and reduce the need for more extensive surgery.
- What could go wrong
- This is a small, early-stage study with only 50 participants, so results may not apply to all patients. Risks include bleeding, pneumothorax, or allergic reaction to the dye.
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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About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2025
An estimate. Start dates often move.
- Expected to finish
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May 2026
An estimate. End dates often move.
- 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 to 80 years
- 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age 18-80 years * Clinically indicated sub-lobar resection * Tolerates general anesthesia * Single/multiple small nodules \<20 mm in peripheral lung field * Nodules difficult to locate intraoperatively by inspection/palpation Exclusion Criteria: * Contraindications to bronchoscopy/anesthesia * Coagulopathy or bleeding tendency * Implanted devices interfering with navigation * Allergy to ICG or iodinated contrast * Pregnant/lactating women * Intraoperative findings not suitable for procedure
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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