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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)

2026年8月24日 更新者: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.

研究概览

地位

尚未招聘

详细说明

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.

研究类型

观察性的

注册 (估计的)

220

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Rosalynn Austin, PhD, RN, BN, MSc, BSc
  • 电话号码:+447531785361
  • 邮箱:rosalynn@zedsen.com

研究联系人备份

  • 姓名:Marc Goldfinger, PhD
  • 电话号码:+447531785361
  • 邮箱:marc@zedsen.com

学习地点

      • London、英国、W6 8RF
        • Imperial College Trust
        • 接触:
          • Adrian Lim, Professor and Consultant Radiologist, MD FRCP FRCR
          • 电话号码:+4420 3313 0764
          • 邮箱:adrian.lim@nhs.net
        • 副研究员:
          • Farah Rehman, MBBS
        • 副研究员:
          • Lesley Honeyfield, BA

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

取样方法

非概率样本

研究人群

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.

描述

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

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
干预/治疗
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.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Breast tissue electrical properties
大体时间: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.

次要结果测量

结果测量
措施说明
大体时间
Breast density electrical properties
大体时间: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
大体时间: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
大体时间: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.

其他结果措施

结果测量
措施说明
大体时间
Exploratory Outcome: Impact of breast density on lesion identification
大体时间: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
大体时间: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
大体时间: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
大体时间: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.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 研究主任:Marc Goldfinger, PhD、Zedsen Limited
  • 首席研究员:Adrian Lim, MD FRCP FRCR、Imperial College NHS Trust

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年9月1日

初级完成 (估计的)

2028年9月1日

研究完成 (估计的)

2028年12月1日

研究注册日期

首次提交

2026年8月17日

首先提交符合 QC 标准的

2026年8月20日

首次发布 (实际的)

2026年8月24日

研究记录更新

最后更新发布 (实际的)

2026年8月27日

上次提交的符合 QC 标准的更新

2026年8月24日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

其他研究编号

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

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

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

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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