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Study identifier: NCT06977698 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: Recruiting

Intra-operative Detection of Positive Margins and Lymph Nodes in Breast Surgery

Condition: Breast Cancer Invasive  ·  Sponsor: University of Nottingham

PhaseN/A
Planned participants120
Who can joinFemale, N/A to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
WhereNottingham, United Kingdom

Interested? Contact the study team ↓

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Professional view of this study — listed sites, countries and recruiting context from the public registry. Everything below is written for patients and caregivers.See where this study is running →

About this study

In this project, the investigators will develop novel optical coherence tomography (OCT)-Raman spectroscopy and autofluorescence (AF)-Raman spectroscopy systems based on a selective sampling approach optimised for high-resolution analysis of whole lumpectomy specimens and sentinel lymph node (SLN) biopsies, respectively. The aim of using optical coherence tomography is not to detect cancer directly, but rather to identify adipose tissue so that large adipose regions can be excluded from subsequent Raman spectroscopy measurements. Although OCT has limited ability to distinguish tumour tissue from the surrounding normal stroma, adipose tissue exhibits a distinctive appearance in optical coherence tomography images because of its low backscattering properties, resulting from adipocytes that are filled with lipids and contain small, flattened nuclei. In contrast, benign dense tissue (stroma, ducts, and lobules) and malignant tissue produce much stronger backscattering signals. These characteristic patterns enable adipose tissue to be distinguished from other breast tissues using classification models based on optical coherence tomography reflectivity profiles, achieving 94% sensitivity and 93% specificity. Excluding adipose tissue from further analysis reduces the number of Raman spectroscopy measurements required, allowing the remaining, smaller tissue regions to be examined to discriminate between benign and malignant tissue. This flexible and adaptable scanning strategy is ex…

This description comes directly from the study's public registry record.

Talk to the study team

Ioan Notingher  ·  0)115 951 3082  ·  ppzin@exmail.nottingham.ac.uk

Nehal Atallah  ·  07521100084  ·  msznma@nottingham.ac.uk

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

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.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (1)

Nottingham university hospitalsNottingham, United KingdomRecruiting

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Nottingham

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