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RECRUITING
NCT07402616
NA

Ex Vivo Cutaneous SCC

Sponsor: Rigshospitalet, Denmark

View on ClinicalTrials.gov

Summary

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.

Official title: Feasibility of 3D ex Vivo Ultrasonography for Post-operative Evaluation of Tumor Margins in Cutaneous Squamous Cell Carcinoma

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2026-02-01

Completion Date

2027-09-01

Last Updated

2026-02-11

Healthy Volunteers

No

Interventions

DIAGNOSTIC_TEST

ex vivo 3D ultrasonography

Surgical specimens scanned with 3D ultrasonography

Locations (1)

Rigshospitalet

Copenhagen, Denmark