Fingernail moons may reveal who responds to breast cancer therapy
NCT ID NCT07590570
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at whether the small white moons at the base of fingernails (lunula) can predict how well breast cancer patients respond to chemotherapy before surgery. Researchers will track 188 patients to see if lunula status is linked to tumor disappearance and side effects. The goal is to find a simple, non-invasive way to personalize treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- neoadjuvant therapy (chemotherapy before surgery)
- What this could lead to
- If successful, this could help doctors predict which breast cancer patients will benefit most from neoadjuvant therapy, personalizing treatment.
- What could go wrong
- This is an observational study, not a treatment trial. The link between lunula status and outcomes is unproven and may not lead to any change in practice.
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.
- Participants
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About 188 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2026
- Expected to finish
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Jan 2033
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.
Who is studied
Breast cancer patients who have received or plan to receive neoadjuvant therapy.
- 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: * Aged 18 years or older * Pathologically confirmed invasive primary breast cancer * Patients who have received or are scheduled to receive neoadjuvant therapy Exclusion Criteria: * De novo stage IV breast cancer
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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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Renji Hospital, School of Medicine, Shanghai Jiaotong University
Shanghai, 200127, China
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Other studies related to the condition(s) this trial covers.
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