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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 août 2026 mis à jour par: 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.

Aperçu de l'étude

Statut

Pas encore de recrutement

Intervention / Traitement

Description détaillée

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.

Type d'étude

Observationnel

Inscription (Estimé)

220

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

  • Nom: Rosalynn Austin, PhD, RN, BN, MSc, BSc
  • Numéro de téléphone: +447531785361
  • E-mail: rosalynn@zedsen.com

Sauvegarde des contacts de l'étude

  • Nom: Marc Goldfinger, PhD
  • Numéro de téléphone: +447531785361
  • E-mail: marc@zedsen.com

Lieux d'étude

      • London, Royaume-Uni, W6 8RF
        • Imperial College Trust
        • Contact:
          • Adrian Lim, Professor and Consultant Radiologist, MD FRCP FRCR
          • Numéro de téléphone: +4420 3313 0764
          • E-mail: adrian.lim@nhs.net
        • Sous-enquêteur:
          • Farah Rehman, MBBS
        • Sous-enquêteur:
          • Lesley Honeyfield, BA

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

Méthode d'échantillonnage

Échantillon non probabiliste

Population étudiée

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.

La description

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

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

Cohortes et interventions

Groupe / Cohorte
Intervention / Traitement
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.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Breast tissue electrical properties
Délai: 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.

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Breast density electrical properties
Délai: 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
Délai: 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
Délai: 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.

Autres mesures de résultats

Mesure des résultats
Description de la mesure
Délai
Exploratory Outcome: Impact of breast density on lesion identification
Délai: 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
Délai: 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
Délai: 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
Délai: 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.

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Les enquêteurs

  • Directeur d'études: Marc Goldfinger, PhD, Zedsen Limited
  • Chercheur principal: Adrian Lim, MD FRCP FRCR, Imperial College NHS Trust

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

1 septembre 2026

Achèvement primaire (Estimé)

1 septembre 2028

Achèvement de l'étude (Estimé)

1 décembre 2028

Dates d'inscription aux études

Première soumission

17 août 2026

Première soumission répondant aux critères de contrôle qualité

20 août 2026

Première publication (Réel)

24 août 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

27 août 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

24 août 2026

Dernière vérification

1 août 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

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

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Description du régime IPD

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

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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