Basal Cell Skin Cancer Clinical Trials

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Multimodal Imaging of Basal Cell Carcinoma: A Usability Study

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY

The goal of this observational study is to evaluate the time efficiency and practical usability of three non-invasive skin imaging tools in adults (18 years and older) with basal cell carcinoma (BCC), the most common type of skin cancer. The main questions it aims to answer are: How long does it take to perform each scan (optical coherence tomography, line-field confocal optical coherence tomography, and high-frequency ultrasound)? How comfortable is each scan for participants? How well do the imaging tools work across different areas of the body? Participants will undergo one study visit of approximately 40 minutes, during which three non-invasive skin scans are performed on the skin lesion. Each scan uses a different imaging tool. Participants will also complete a short questionnaire about their experience. No biopsies or other invasive procedures are performed as part of the study.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age 18 years or older Presence of a histologically confirmed or clinically suspected basal cell carcinoma lesion scheduled for standard clinical management Ability to provide written informed consent

Locations
Other Locations
Denmark
Department of Dermatology, Bispebjerg Hospital
RECRUITING
Copenhagen
Contact Information
Primary
Otto Dideriksen, MD
otto.dideriksen@regionh.dk
+45 29103585
Backup
Emilie Ravn, Project Nurse
emilie.sylvestersen.ravn.02@regionh.dk
+45 38635362
Time Frame
Start Date: 2026-09-14
Estimated Completion Date: 2027-11-05
Participants
Target number of participants: 50
Treatments
BCC Participants
Adults aged 18 years or older with histologically confirmed or clinically suspected basal cell carcinoma scheduled for standard clinical management at the Department of Dermatology, Bispebjerg Hospital, Copenhagen, Denmark. Each participant undergoes a single study visit comprising sequential non-invasive imaging with three AI-assisted modalities: optical coherence tomography (OCT), line-field confocal optical coherence tomography (LC-OCT), and high-frequency ultrasound (HFUS). No interventions are performed. All imaging is adjunct to standard care.
Related Therapeutic Areas
Sponsors
Leads: Bispebjerg Hospital

This content was sourced from clinicaltrials.gov