New mapping technique aims to prevent arm swelling after breast cancer surgery
NCT ID NCT00572481
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests a technique called axillary reverse mapping during breast cancer surgery. Doctors inject a radioactive tracer and blue dye to map the arm's lymph drainage, hoping to avoid damaging those vessels and reduce the risk of lymphedema (arm swelling). The study involves 1,000 participants and will track swelling for one year after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Axillary reverse mapping procedure using technetium-99m sulfur colloid and blue dye
- What this could lead to
- If successful, this technique could reduce the risk of lymphedema after breast cancer surgery, improving long-term quality of life.
- What could go wrong
- This is a phase 2 study, so results are still preliminary. The technique may not significantly lower lymphedema risk, and there are standard surgical risks.
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
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
About 1,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
May 2007
- Expected to finish
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Nov 2027
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 years and older
- Sex
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Anyone
- Healthy volunteers
-
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: * 18-100 years old * Not pregnant or breastfeeding * Breast cancer requiring lymph node evaluation for the ipsilateral or contralateral breast OR prophylactic mastectomy * Willing participation following an informed consent process Exclusion Criteria: * Patient \< 18 y/o or \> 100 y/o * Pregnant or breastfeeding * If a pregnant female should be diagnosed with breast cancer an exception would be considered on a case to case basis.
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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
-
University of Arkansas For Medical Sciences
Little Rock, Arkansas, 72205, United States
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