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An Investigation Into Dielectric Testing for the Evaluation and Characterisation of Breast Tissue Using a Novel Time-Domain Bioimpedance Tool (DiTECT)

24. august 2026 oppdatert av: Zedsen Limited

Capacitance measures a material's ability to store the movement of electrical energy in the electric field. Different of the human body are known to have different capacitance values. Research is looking into utilising capacitance differences, using a method called bioimpedance, to detect signatures of cancer. Breast cancer is the most common type of cancer in women globally, and the bioimpedance of healthy breast tissue is different to cancer tissue. Breast tissue is accessible by non-invasive means and has well-established clinical tools for cancer detection. However, results from studies vary and research is needed to understand how bioimpedance can be used in cancer research and the development of less invasive detection tools.

Zedsen Limited developed the time-domain bioimpedance sensing (TD-BIS) scanner capable of measuring capacitance. Previous versions of the TD-BIS scanner were investigated in a proof-of-concept study and shown to be safe to use. The proposed study aims to establish the feasibility, safety, and performance of the updated TD-BIS scanner in classifying healthy, benign, and cancer tissue. We will recruit 220 women attending a breast appointment at Charing Cross Hospital (40 without lesions, and 90 with malignant lesions and 90 with benign lesions). Invited women will have their breasts scanned after routine imaging and before any biopsy. Data will be fed into AI algorithms to enhance the TD-BIS scanner performance. The TD-BIS scanner's ability to measure capacitance of tumours that are being treated with neoadjuvant chemotherapy will be explored. Twenty women with a malignancy who consent to being followed up over their treatment course, will have 2 additional scans. Finally, participants will be asked to share their experience of the TD-BIS scanner in a questionnaire. Results from this study can further our understanding on how capacitance and such devices can be used in breast cancer clinical management.

Studieoversikt

Status

Har ikke rekruttert ennå

Forhold

Intervensjon / Behandling

Detaljert beskrivelse

Zedsen Limited has manufactured a TD-BIS scanner, which can measure electrical properties of different human tissue types. The equipment consists of two operational parts: a Charging Cradle and a Sensor Head. The Sensor Head is used to perform measurements on a client's breast. The Charging Cradle is used to charge and hold the Sensor Head between and after measurements, as well as to enable data transfer. A computerised system runs the TD-BIS scanner's associated Application (App) will guide the clinical user on completing the breast scan to ensure complete data collection.

The TD-BIS scanner capable of measuring electrical properties of breast tissue. A preliminary study in the UK evidenced the TD-BIS scanner's ability to identify lesions from healthy breast tissue based on differences in tissue electrical properties. In the proof-of-concept study, the TD-BIS scanner was able to identify invasive lesion, in situ lesions and benign breast changes (including cysts, AIDEP and fibroadenoma) ranging in size from as small as 0.5cm3 to larger than 1.5cm3. Further, the accuracy of lesion detection was impaired in breasts with higher density (BI-RAD scores C and D) . The proposed study aims to further investigate and validate previous results by utilising the TD-BIS scanner on a larger, more diverse cohort of patients and while exploring the effects of breast density on lesion detection.

Breast density is the amount of fibroglandular tissue compared with the amount of fatty tissue in the breast . Breast density if currently classified using a mammogram (MMG) according to the 4-point BI-RADS breast density category: A, entirely fatty; B, scattered areas of fibroglandular density; C, heterogeneously dense; D, extremely dense. Higher breast density (BI-RADS category of C or D) is a known risk factor for breast cancer .

MMG is the gold standard imaging modality used in breast cancer screening and diagnosis . While it contributes to increased survival rates of breast cancer patients through early detection, it has many limitations including exposure to ionising radiation, patient discomfort, and most notably, a decreased sensitivity in dense breasts. Just under half of all women, particularly those who are younger, pre- or perimenopausal or women of colour; have more dense breasts. Other imaging modalities such as Magnetic Resonance Imaging (MRI) and ultrasound are less affected by breast density but are limited by other factors such as accessibility, costs, semi-quantitative results and high false positive rates.

Dielectric imaging is emerging as a promising technique for breast cancer detection. As a principle it uses differences in electric properties called capacitance, specifically permittivity and conductivity, which measure any materials ability to store of move energy. There are cellular differences between breast tissue types (no-lesion, benign or malignant lesions) which has been shown to have an impact on the bioelectric properties. There is some evidence to suggest that this way of imaging a breast may also overcome some of the MMG limitations of detecting breast tissue types, within dense breasts. But these systems still require specialist equipment within hospitals.

Further, the existing method used to evaluate tumour response to neoadjuvant chemotherapy, is subjective. The response evaluation criteria in solid tumours (RECIST) 1.1 is the standard method used. It requires an experienced radiologist to choose the target lesions and measure changes in tumour size before and after treatment. The methods is limited due to inherent variability and errors in reported related to clinical efficacy, as well as only capturing size differences with no way to capture the change in tumour microstructure that occurs with effective treatment.

The prototype TD-BIS scanner was shown to capture the bioelectric signal of various types of breast tissue types in the first-in-human study. The prototype device has been refined in collaboration with clinical users and the proposed study will now invite a larger population of women who are attending a breast health clinic to be scanned with the TD-BIS scanner in addition to their standard of care breast health clinic appointment. Clinicians and patients will be blinded to the TD-BIS scanner outputs, and their clinical findings and results will be used as the ground truth.

The aim of the study is to determine the feasibility of using the improved TD-BIS scanner to identify the electrical properties of various breast tissues types. It will also be evaluated for its ability to classify breast density, differentiate lesion type, and the safety and tolerability of the device in a UK clinical population.

Studietype

Observasjonsmessig

Registrering (Antatt)

220

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

  • Navn: Rosalynn Austin, PhD, RN, BN, MSc, BSc
  • Telefonnummer: +447531785361
  • E-post: rosalynn@zedsen.com

Studer Kontakt Backup

  • Navn: Marc Goldfinger, PhD
  • Telefonnummer: +447531785361
  • E-post: marc@zedsen.com

Studiesteder

      • London, Storbritannia, W6 8RF
        • Imperial College Trust
        • Ta kontakt med:
          • Adrian Lim, Professor and Consultant Radiologist, MD FRCP FRCR
          • Telefonnummer: +4420 3313 0764
          • E-post: adrian.lim@nhs.net
        • Underetterforsker:
          • Farah Rehman, MBBS
        • Underetterforsker:
          • Lesley Honeyfield, BA

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

Eligible people will be identified from those attending their breast clinic appointment who will be having, or had a mammogram or ultrasound, will be identified by a member of the clinical team.

Patients eligible for the NACT sub-study may be identified by two routes: first, participants already enrolled in the main DiTECT study whose malignancy is subsequently confirmed and whose clinical plan is to receive standard-of-care neoadjuvant chemotherapy. Second, patients newly diagnosed with invasive breast cancer at the participating site (including those not previously recruited to the main study) who are identified following routine NHS triple assessment, histological confirmation, multidisciplinary team review, and who are scheduled to commence standard-of-care neo-adjuvant chemotherapy. Those who are eligible for the study will only be approached after the cancer diagnosis at which time they will also receive trial documents.

Beskrivelse

Inclusion Criteria:

  • Attending a breast clinic appointment or other appointment at a participating site
  • Assigned female sex at time of birth
  • Aged 18 years or older at time of scan
  • Willing, able and mentally competent to read, understand, and provide informed consent in English

    • Patients who wish to enter the NACT sub-study, inclusion in NACT care is required.

Exclusion Criteria:

  • Participants who have undergone biopsy less than 14 days before the TD-BIS scanner session
  • Participants with implanted electronics anywhere in the body
  • Participants with breast implants
  • Participants with nipple piercings (unless they are removed prior to the scan)
  • Participants who are lactating
  • Pregnant participants by verbal confirmation
  • Participants with pacemakers
  • Participants with open breast wound
  • Participants who had previous breast surgery (mastectomy, lumpectomy)
  • Participants who have breast lesion localisation device (i.e., wire, seed, Magseed)

    *Patients who wish to enter the NACT sub-study, there is one additional exclusion criteria:

  • Participants who have any breast surgery prior to the second scan

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Kohorter og intervensjoner

Gruppe / Kohort
Intervensjon / Behandling
Benign Lesions
Participants with clinically identified benign lesions
Participants will all receive a scan of their breast with the TD-BIS device. This is not an intervention it is an additional non-invasive device with a novel device that is hand-held with non-ionising radiation. The scan with the device will be a research observation which will be performed to test the feasibility and accuracy of the device in this population.
Malignant Lesions
Participants with clinically identified malignant lesions
Participants will all receive a scan of their breast with the TD-BIS device. This is not an intervention it is an additional non-invasive device with a novel device that is hand-held with non-ionising radiation. The scan with the device will be a research observation which will be performed to test the feasibility and accuracy of the device in this population.
No Lesions
Participants with no clinically identified lesions
Participants will all receive a scan of their breast with the TD-BIS device. This is not an intervention it is an additional non-invasive device with a novel device that is hand-held with non-ionising radiation. The scan with the device will be a research observation which will be performed to test the feasibility and accuracy of the device in this population.
NACT sub-study
Participants from the malignant lesion cohort who agree to additional TD-BIS scanner sessions during their NACT treatment (pre-, mid-, and post- treatment).
Participants will all receive a scan of their breast with the TD-BIS device. This is not an intervention it is an additional non-invasive device with a novel device that is hand-held with non-ionising radiation. The scan with the device will be a research observation which will be performed to test the feasibility and accuracy of the device in this population.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Breast tissue electrical properties
Tidsramme: Enrollment to the end of the study, anticipated to be 24 months.
Establish electrical properties of healthy, benign, and malignant tissue associated with the TD-BIS scanner.
Enrollment to the end of the study, anticipated to be 24 months.

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Breast density electrical properties
Tidsramme: Enrollment to end of study, anticipated to be 24 months.
Establish electrical properties of different breast densities reported in Breast-imaging-reporting and Data system (BI-RADS) density category.
Enrollment to end of study, anticipated to be 24 months.
Electrical properties of benign and malignant tissues by breast density
Tidsramme: Enrollment to end of study, anticipated to be 24 months.
Establish electrical properties of benign and malignant tissue in all BI-RADS density category.
Enrollment to end of study, anticipated to be 24 months.
Safety of the TD-BIS scanner
Tidsramme: Enrollment to end of study, anticipated to be 24 months.
Evaluate the safety of the TD-BIS scanner alongside patient tolerability and clinical usability.
Enrollment to end of study, anticipated to be 24 months.

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Exploratory Outcome: Impact of breast density on lesion identification
Tidsramme: Enrollment to end of study, anticipated to be 24 months.
Evaluate clinical parameters between benign and malignant tissue and the impact of breast density
Enrollment to end of study, anticipated to be 24 months.
Exploratory outcome: Changes in the electrical properties of a malignant lesions
Tidsramme: Enrollment to end of study, anticipated to be 24 months.
Evaluation of changes in scanner-derived electrical properties following Standard of Care (SOC) intervention for patients receiving Neoadjuvant Chemotherapy (NACT)
Enrollment to end of study, anticipated to be 24 months.
Feasibility Outcome: Recruitment feasibility
Tidsramme: Enrollment to end of study, anticipated to be 24 months.
Establish the research screening and recruitment characteristics to describe feasibility of recruitment related to current eligibility criteria
Enrollment to end of study, anticipated to be 24 months.
Feasibility Outcome: Patient experience
Tidsramme: Enrollment to end of study, anticipated to be 24 months.
Establish the ability to capture patient experience with the TD-BIS scanner using the adapted TMI.
Enrollment to end of study, anticipated to be 24 months.

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Samarbeidspartnere

Etterforskere

  • Studieleder: Marc Goldfinger, PhD, Zedsen Limited
  • Hovedetterforsker: Adrian Lim, MD FRCP FRCR, Imperial College NHS Trust

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. september 2026

Primær fullføring (Antatt)

1. september 2028

Studiet fullført (Antatt)

1. desember 2028

Datoer for studieregistrering

Først innsendt

17. august 2026

Først innsendt som oppfylte QC-kriteriene

20. august 2026

Først lagt ut (Faktiske)

24. august 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

27. august 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

24. august 2026

Sist bekreftet

1. august 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • ZED-DiTECT-PROT-001
  • IRAS 370214 (Annen identifikator: Health Research Authority (HRA))
  • 26/EE/0128 (Annen identifikator: East of England - Cambridge East Research Ethics Committee)
  • CI-2026-0035-GB (Annen identifikator: Medicines and Healthcare Products Regulatory Agency)

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

IPD-planbeskrivelse

Participant consent for widespread and open sharing of data was not part of the ethical review and approval.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .