Actively Recruiting
Ex Vivo Cutaneous SCC
Led by Rigshospitalet, Denmark · Updated on 2026-02-11
30
Participants Needed
1
Research Sites
82 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a prospective study including patients ( ≥ 18 years) referred for surgical treatment of primary cutaneous squamous cell carcinoma at the Department of Plastic Surgery, Rigshospitalet. After written and informed consent, patients will undergo standard surgical excision, followed by ex vivo 3D ultrasonography of the specimen using a 3Sonic device connected to a high-frequency ultrasound machine. This will create 3D ultrasound tomographic scans which will be interpreted by one investigator blinded to histopathology. The investigated outcomes will primarily be the deep margin distance. This will be compared to histopathology, where a pathologist - blinded to the ultrasonography results - will slice the entire specimen parallel to the ultrasound images. A third investigator will then match the histopathology images to the ultrasound images for correlation of the measured deep margins.
CONDITIONS
Official Title
Ex Vivo Cutaneous SCC
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults with primary cutaneous squamous cell carcinoma.
You will not qualify if you...
- Carcinomas located on the eyelids, vulva, penis, or perianal.
- Tumors with an anticipated excision larger than 60mm.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Rigshospitalet
Copenhagen, Denmark, 2100
Actively Recruiting
Research Team
L
Linnea Langhans, MD, PhD
CONTACT
M
Martin Garset-Zamani, MD, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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