Glowing dye could replace radioactive markers for breast cancer surgery
NCT ID NCT03313908
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a fluorescent dye called indocyanine green (ICG) can help surgeons locate small, non-palpable breast tumors during surgery. Ten women with early-stage breast cancer received both the dye and a standard radioactive seed, and doctors compared how well each method pinpointed the tumor. The goal is to see if ICG could replace the radioactive method, making the procedure simpler and more comfortable for patients.
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)
- What this could lead to
- If successful, this could offer a simpler, non-radioactive way to locate small breast tumors during surgery, improving patient comfort and hospital logistics.
- What could go wrong
- This is a very small feasibility study with only 10 participants, so results may not apply broadly. The technique may not be as accurate as the current standard.
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
-
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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10 people
The number who actually took part.
- Started
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Oct 2017
- Finished
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Dec 2018
- Lead sponsor
-
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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Female participants only
- 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: * Woman Age ≥ 18 years * Non-palpable tumor * Single tumor * First breast surgery * Histology: ductal carcinoma * Written consent * Being affiliated or benefiting from a French social security system Exclusion Criteria: * palpable tumor * multifocal tumor * antecedent of breast surgery
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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
-
UH Montpellier
Montpellier, 34295, France
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Other studies related to the condition(s) this trial covers.
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