An observational study in Breast Cancer and Breast - Female, sponsored by Zedsen Limited. Recruiting at 1 site in United Kingdom. Open to female participants aged 18 Years to 85 Years. Per ClinicalTrials.gov, last updated 2026-09-30.
Sponsored by Zedsen Limited · Observational
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Among 757 studies in Breast Neoplasms with a site in United Kingdom — 98 open to participants now, 196 under way, 67 of them phase 3. Breast Neoplasms · United Kingdom.
Among the 757 studies in Breast Neoplasms with a site in United Kingdom, this one is the 62nd largest by planned enrollment of the 122 observational ones that give a count, is one of 13 that started in 2026, is one of 123 observational ones, reaches primary completion later than 153 of the 195 other live ones, and was the 756th registered.
14,829 studies on the registry are indexed under Breast Neoplasms; 3,318 are open to participants now.
Browse Breast Neoplasms studies →98 of the 757 studies in Breast Neoplasms with a site in United Kingdom are open now. Recruiting first, the newest first:
University Hospitals of North Midlands NHS Trust · Sites in United Kingdom
Ages 18+ · Women only
Imperial College London · Sites in United Kingdom
Ages 16–100
BeOne Medicines · Sites in United Kingdom, United States, Australia and 13 more countries
Ages 18+
Hoffmann-La Roche · Sites in United Kingdom, United States, Argentina and 23 more countries
Ages 18+
AstraZeneca · Sites in United Kingdom, United States
Ages 18+ · Women only
A study can be open while its sites in United Kingdom have not opened yet or have stopped. Only those recruiting at a site in United Kingdom →
Of the 2,398 Breast Neoplasms studies recruiting now, 1,569 (65%) set no upper age limit and 592 (25%) stop at 75 or younger; 103 take children under 18; 215 take healthy volunteers.
This study: 18 Years to 85 Years · female · no healthy volunteers.
The full table on the hub →This tab as a report to print or save as PDF → With an account.
757 studies; the count open now beside each. This study's row is marked.
A study in two phases is counted once above. Listed by phase, each with its combined phases: Phase 1 125 · Phase 2 238 · Phase 3 229 · Phase 4 7
First in 1987; this study’s year is marked. 13 started in 2026.
By drug class, each counting the studies that test any of its medicines:
This study's planned enrollment of 220 is above the median of 184 across 3,235 observational studies indexed under Breast Neoplasms.
Median enrollment 221 across the 613 interventional studies, 221 across the 122 observational. Of the 451 that completed or were terminated, 201 (45%) have results posted.
This tab as a report to print or save as PDF → With an account.
422 of 757 have an industry lead sponsor. The 10 most frequent:
Zedsen Limited is the lead sponsor of 2 studies on the registry; 2 are open to participants now.
Zedsen Limited has 2 studies filed under Breast Neoplasms — fewer than ten, so there is no comparison to draw.
49 of the studies in Breast Neoplasms with a site in United Kingdom that are under way reach primary completion within a year, 14 of them phase 3. Phase 3 first, then by date:
| Study | Primary completion |
|---|---|
| NCT05646862Phase 3Hoffmann-La RocheA Study Evaluating the Efficacy and Safety of Inavolisib Plus Fulvestrant Compared With Alpelisib Plus Fulvestrant in Participants With HR-Positive, HER2-Negative, PIK3CA Mutated, Locally Advanced or Metastatic Breast Cancer Post CDK4/6i and Endocrine Combination Therapy | 2026-11-13 |
| NCT05894239Phase 3Hoffmann-La RocheA Study to Evaluate the Efficacy and Safety of Inavolisib in Combination With Phesgo Versus Placebo in Combination With Phesgo in Participants With PIK3CA-Mutated HER2-Positive Locally Advanced or Metastatic Breast Cancer | 2026-12-31 |
| NCT04873362Phase 3Hoffmann-La RocheA Study Evaluating the Efficacy and Safety of Adjuvant Atezolizumab or Placebo and Trastuzumab Emtansine for Participants With HER2-Positive Breast Cancer at High Risk of Recurrence Following Preoperative Therapy | 2027-03-31 |
| NCT05696626Phase 3LeonaBioEvaluation of Lasofoxifene Combined With Abemaciclib Compared With Fulvestrant Combined With Abemaciclib in Locally Advanced or Metastatic ER+/HER2- Breast Cancer With an ESR1 Mutation | 2027-04 |
| NCT04421963Phase 3AstraZenecaRoll Over StudY for Patients Who Have Completed a Previous Oncology Study With Olaparib | 2027-04-06 |
Add all 49 to your calendar (.ics) → With an account.
Among the 757 studies in Breast Neoplasms with a site in United Kingdom, from their registry updates:
This tab as a report to print or save as PDF → With an account.
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.
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.
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.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Willing, able and mentally competent to read, understand, and provide in English
Exclusion Criteria:
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:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
A biopsy takes a small piece of tissue to examine. “Archival tissue” is a sample already taken, for example at diagnosis, and kept by the hospital.
Whether a stored sample will do depends on when it was taken, how much there is and what the study needs. Ask whether the study accepts your stored sample or needs a new biopsy.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Biopsy and archival tissue
A biopsy takes a small piece of tissue to examine. “Archival tissue” is a sample already taken, for example at diagnosis, and kept by the hospital.
Whether a stored sample will do depends on when it was taken, how much there is and what the study needs. Ask whether the study accepts your stored sample or needs a new biopsy.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Participants with clinically identified benign lesions
Device: TD-BIS scanner
Participants with clinically identified malignant lesions
Device: TD-BIS scanner
Participants with no clinically identified lesions
Device: TD-BIS scanner
Participants from the malignant lesion cohort who agree to additional TD-BIS scanner sessions during their NACT treatment (pre-, mid-, and post- treatment).
Device: TD-BIS scanner
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.
Breast tissue electrical properties
Establish electrical properties of healthy, benign, and malignant tissue associated with the TD-BIS scanner.
Time frame: Enrollment to the end of the study, anticipated to be 24 months.
Breast density electrical properties
Establish electrical properties of different breast densities reported in Breast-imaging-reporting and Data system (BI-RADS) density category.
Time frame: Enrollment to end of study, anticipated to be 24 months.
Electrical properties of benign and malignant tissues by breast density
Establish electrical properties of benign and malignant tissue in all BI-RADS density category.
Time frame: Enrollment to end of study, anticipated to be 24 months.
Safety of the TD-BIS scanner
Evaluate the safety of the TD-BIS scanner alongside patient tolerability and clinical usability.
Time frame: Enrollment to end of study, anticipated to be 24 months.
Exploratory Outcome: Impact of breast density on lesion identification
Evaluate clinical parameters between benign and malignant tissue and the impact of breast density
Time frame: Enrollment to end of study, anticipated to be 24 months.
Exploratory outcome: Changes in the electrical properties of a malignant lesions
Evaluation of changes in scanner-derived electrical properties following Standard of Care (SOC) intervention for patients receiving Neoadjuvant Chemotherapy (NACT)
Time frame: Enrollment to end of study, anticipated to be 24 months.
Feasibility Outcome: Recruitment feasibility
Establish the research screening and recruitment characteristics to describe feasibility of recruitment related to current eligibility criteria
Time frame: Enrollment to end of study, anticipated to be 24 months.
Feasibility Outcome: Patient experience
Establish the ability to capture patient experience with the TD-BIS scanner using the adapted TMI.
Time frame: Enrollment to end of study, anticipated to be 24 months.
Plan to share: No — Participant consent for widespread and open sharing of data was not part of the ethical review and approval.
Start is estimated for Sep 2026; primary completion for Sep 2028, 24 months later.
How these figures are worked out, and which studies are left out of them.
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
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Zedsen Limited