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Terabotics - terahertz robotics for surgery and medicine

TERAhertz roBOTICS for surgery and medicine

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN17256655
Enrollment
100
Registered
2024-08-05
Start date
2024-10-01
Completion date
Unknown
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Identifying and assessing the extent suspected skin cancer defined as Basal Cell Carcinoma, Lentigo Maligna or Melanoma in Situ in patients scheduled to have a surgical excision. Cancer

Interventions

Participants scheduled to have a surgical excision will undergo the study procedures on the day of their operation, prior to the surgical procedure. Firstly, participants will have their area of inte
once to acquire images of a control area similar to the area of interest, but clinically free from obvious pathology
and lastly they will undergo a scan of the area of interest (suspected skin cancer). A good quality scan will be needed from each area, and may need repeating if the signal acquisition is inadequate.

Sponsors

University Hospitals Coventry and Warwickshire NHS Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. NHS patients attending University Hospitals Coventry and Warwickshire 2. Area of interest accessible for THz scan 3. Aged 18 years and over 4. Suspected skin cancer defined as: 4.1. lesions clinically suspicious for Basal Cell Carcinoma (BCC) 4.2. biopsy proven BBC 4.3. biopsy proven Lentigo Maligna (LM) 4.4. Melanoma in Situ (MiS) 5. Capacity to give informed consent

Exclusion criteria

Exclusion criteria: 1. Confirmed biopsy proven other skin cancer at the same area of interest 2. Absence of suspected or confirmed skin cancer as described in the inclusion criteria 3. Unable to consent to the study

Design outcomes

Primary

MeasureTime frame
Measured at baseline using the screening/recruitment log which clinical research staff will manage, collated safety monitoring reports (AEs/SAEs) and study database output: 1.Number of patients screened, eligible, recruited and withdrawn 2.Patient willingness to participate in the trial 3.Participant tolerance of the device 4.Number of participants with complete datasets

Secondary

MeasureTime frame
1. Terahertz scan data and the formal reported histological analysis as part of the standard skin cancer management pathway 2. Histology results collected post-surgery

Countries

England, United Kingdom

Contacts

Public ContactCristiana Huhulea
cristiana.huhulea@uhcw.nhs.uk+44 24 7696 7476

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026