Can a smart light beam help surgeons remove every last cancer cell?
NCT ID NCT06977698
First seen Jul 30, 2026 · Last updated Jul 31, 2026 · Updated 1 time
Summary
This trial is testing a new imaging system that combines two types of light-based technology to help surgeons see if any cancer cells remain at the edges of removed breast tissue during surgery. The goal is to reduce the need for repeat operations. About 120 people undergoing breast-conserving surgery will take part, and the system will be evaluated for speed and accuracy.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a multimodal spectroscopic imaging system combining optical coherence tomography (OCT) and Raman spectroscopy
- What this could lead to
- If successful, this approach could help surgeons remove all cancerous tissue in one operation, reducing the need for follow-up surgeries.
- What could go wrong
- This is an early-stage feasibility study, so the technology may not prove accurate enough in real-time surgery. The system also requires further refinement before it could be widely used.
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 120 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2023
- Expected to finish
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Apr 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.
Who is studied
Patients undergoing Wide Local Excision (WLE) for breast cancer at the Breast Cancer Institute, Nottingham City Hospital.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- 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 * Patients undergoing breast surgery wide local excision (WLE). * Able to give informed consent. * Any age. Exclusion criteria • Patients where there is any doubt regarding the diagnosis from pathologist as ascertained by previous diagnostic biopsy.
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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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Nottingham university hospitals
RECRUITINGNottingham, United Kingdom
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