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Breast CancerDiTECTNCT07782814

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

An observational study of Breast Cancer and Breast - Female, run by Zedsen Limited at 1 site in United Kingdom.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 to 85 years, women only
Conditions the study is for
Breast Cancer, Breast - Female
What is being tested?
TD-BIS scanner
Type of treatment
Medical device
How many people
220 participants
Where
1 siteUnited Kingdom
Study dates
30 Sep 2026to Dec 2028
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 85 years
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Study population: 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.

Who may be able to join

  • 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.

Who cannot join

  • 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
Show all 12Show fewer
  • 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

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Rosalynn Austin, PhD, RN, BN, MSc, BSc contact

+447531785361

rosalynn@zedsen.com

Marc Goldfinger, PhD contact

+447531785361

marc@zedsen.com

United Kingdom1 site, 1 recruiting
  • Imperial College Trust

    London, W6 8RF

    Adrian Lim, Professor and Consultant Radiologist, MD FRCP FRCR, +4420 3313 0764, adrian.lim@nhs.net

    Farah Rehman, MBBS

    Recruiting

Other trials in United Kingdom

About this study

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.

Read the detailed description

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.

Being tested
TD-BIS scanner
Keywords
Cancer Screening, Breast Screening, Breast Tissue, Capacitance, Breast Density, Medical Device
Medical subject headings
Breast Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • TD-BIS scannerDevice

    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.

Study groups in NCT07782814
Study groupRoleWhat they receive
Benign LesionsParticipants with clinically identified benign lesions
Receives: Device: TD-BIS scanner
Malignant LesionsParticipants with clinically identified malignant lesions
Receives: Device: TD-BIS scanner
No LesionsParticipants with no clinically identified lesions
Receives: Device: TD-BIS scanner
NACT sub-studyParticipants from the malignant lesion cohort who agree to additional TD-BIS scanner sessions during their NACT treatment (pre-, mid-, and post- treatment).
Receives: Device: TD-BIS scanner

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Breast tissue electrical properties

    Establish electrical properties of healthy, benign, and malignant tissue associated with the TD-BIS scanner.

    Measured: Enrollment to the end of the study, anticipated to be 24 months.

Secondary outcomes (3)
  1. Breast density electrical properties

    Establish electrical properties of different breast densities reported in Breast-imaging-reporting and Data system (BI-RADS) density category.

    Measured: Enrollment to end of study, anticipated to be 24 months.

  2. Electrical properties of benign and malignant tissues by breast density

    Establish electrical properties of benign and malignant tissue in all BI-RADS density category.

    Measured: Enrollment to end of study, anticipated to be 24 months.

  3. Safety of the TD-BIS scanner

    Evaluate the safety of the TD-BIS scanner alongside patient tolerability and clinical usability.

    Measured: Enrollment to end of study, anticipated to be 24 months.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Aug 2026
  2. Study start30 Sep 2026 (estimated)
  3. Primary completionSep 2028 (estimated)
  4. Study completionDec 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
220 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07782814
Sponsor's protocol ID
ZED-DiTECT-PROT-001
Other IDs
IRAS 370214, 26/EE/0128, CI-2026-0035-GB
Acronym
DiTECT
Status last verified
Sep 2026
First submitted
17 Aug 2026
Last updated
30 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Participant consent for widespread and open sharing of data was not part of the ethical review and approval.

Publications

  • Beaumont H, Cantini L, Saini KS, Faye N, Gill R, Iannessi A. What are RECIST 1.1 progressions made of? Variability in double-read oncology trials. Eur Radiol. 2026 Jul;36(7):6159-6169. doi: 10.1007/s00330-025-12234-4. Epub 2026 Feb 9.

    PubMed 41663830
  • Nazari SS, Mukherjee P. An overview of mammographic density and its association with breast cancer. Breast Cancer. 2018 May;25(3):259-267. doi: 10.1007/s12282-018-0857-5. Epub 2018 Apr 12.

    PubMed 29651637
  • Moore JX, Han Y, Appleton C, Colditz G, Toriola AT. Determinants of Mammographic Breast Density by Race Among a Large Screening Population. JNCI Cancer Spectr. 2020 Feb 26;4(2):pkaa010. doi: 10.1093/jncics/pkaa010. eCollection 2020 Apr.

    PubMed 32373777
  • Vachon CM, van Gils CH, Sellers TA, Ghosh K, Pruthi S, Brandt KR, Pankratz VS. Mammographic density, breast cancer risk and risk prediction. Breast Cancer Res. 2007;9(6):217. doi: 10.1186/bcr1829.

    PubMed 18190724

Questions about this trial

What is this clinical trial studying?

An observational study of Breast Cancer and Breast - Female, run by Zedsen Limited at 1 site in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 12 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 30 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Rosalynn Austin, PhD, RN, BN, MSc, BSc (+447531785361, rosalynn@zedsen.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Breast tissue electrical properties (time frame: Enrollment to the end of the study, anticipated to be 24 months.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07782814, which also lists 4 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Sep 2026; AzTrials last refreshed its copy on 26 Oct 2026.

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