Blue light therapy could speed healing of breast abscesses
NCT ID NCT07179003
First seen Jun 26, 2026 · Last updated Aug 20, 2026 · Updated 2 times
Summary
This phase 2 study tests whether adding methylene blue photodynamic therapy (MB-PDT) to standard drainage helps breast abscesses heal faster. Fifty adults with breast abscesses will either receive standard drainage alone or drainage plus MB-PDT. The main goal is to see how quickly symptoms like pain and fever go away.
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 photodynamic therapy (MB-PDT)
- What this could lead to
- If it works, this could offer a faster, more effective way to clear breast abscesses and reduce the need for repeat procedures.
- What could go wrong
- This is a small, early-phase trial with only 50 participants. The added light therapy may not improve outcomes over standard drainage alone and could cause discomfort or skin reactions.
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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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- 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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Jul 2027
An estimate. Start dates often move.
- Expected to finish
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Jun 2032
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
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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: * Adults 18 years or older * Clinical signs of breast abscess, including pain, redness, and/or heat of the breast * Approval by the primary care team to pursue PDT and discuss enrollment with the patient Exclusion Criteria: * Pregnancy * Lactation * Allergy to contrast media, narcotics, sedatives, atropine or eggs * Necrotic tissue that requires surgical debridement * Severely compromised cardiopulmonary function or hemodynamic instability * Thrombocytopenia (\<50,000/mm3) * Uncorrectable coagulopathy * Poor kidney function (serum creatinine \>3mg/dl) * Glucose-6-phosphate dehydrogenase (G6PD) deficiency * Patients with hidradenitis suppurativa * Patients with granulomatous mastitis * Unable or unwilling to understand or to provide informed consent * Unable or unwilling to undergo study procedures * Patient unable to cooperate with, or to be positioned for the procedure * Unable to comply with necessary follow up
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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 places running it
1 site. The list below names each one and where it is.
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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.
Contacts and locations
Locations
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University of Rochester Medical Center
Rochester, New York, 14642, United States
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