Blue dye and radioactive tracer team up to spot cancer spread
NCT ID NCT00314405
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested a combination of two methods—radioactive isotope and blue dye injection—to locate sentinel lymph nodes in 100 breast cancer patients. The goal was to see if using both together improves accuracy and cost-effectiveness. Researchers compared the results and analyzed the economic impact of the procedure.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- methylene blue dye and rhenium sulfide isotope
- What this could lead to
- If successful, this could lead to a more accurate and cost-effective way to identify sentinel lymph nodes in breast cancer surgery.
- What could go wrong
- This is a small, completed study with 100 patients, so results may not apply to all breast cancer cases. The methods are already in use, so major breakthroughs are unlikely.
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 100 people
The number the study aims to enrol. It can still change while the study runs.
- Start date
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Apr 2006
- Finished
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Apr 2008
- 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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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.
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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: * patients with infiltrative breast cancer (diagnosed pre-operatively by core biopsy) * approval and informed consent Exclusion Criteria: * chemotherapy * locoregional radiotherapy * prevalent axillary lymph node
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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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Service de Gynécologie-Obstétrique, Hôpital Civil
Strasbourg, 67091, France
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Other studies related to the condition(s) this trial covers.