Actively Recruiting
EU Post-Market Registry to Collect Real-World Clinical Data on the Use of the Histolog Scanner.
Led by SamanTree Medical SA · Updated on 2026-03-05
5000
Participants Needed
1
Research Sites
525 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this observational study is to gather real-world evidence on the performance and safety of the Histolog® Scanner (HLS) when used as intended. HLS is a real-time ex-vivo tissue imaging device.
CONDITIONS
Official Title
EU Post-Market Registry to Collect Real-World Clinical Data on the Use of the Histolog Scanner.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years old at the time of consenting
- Undergoing a surgery or a medical procedure with use of Histolog4 Scanner
- Ability to understand and the willingness to sign a written informed consent.
You will not qualify if you...
- Active participation in a drug, device, or other medical intervention study that has not reached its primary endpoint at the time of consenting
- Patients under judicial protection, legal guardianship or curatorship.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Royal Surrey County Hospital NHS Foundation Trust
Guildford, United Kingdom, GU2 7XX
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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