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EU Post-Market Registry to Collect Real-World Clinical Data on the Use of the Histolog Scanner.

Sponsor: SamanTree Medical SA

NCT ID: NCT07006090

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Histolog Scanner (device)
How long the study runs
Study runs about 121 months (dates as stated)
About the drug or intervention
Histolog Scanner — device: Histolog Scanner intended to allow imaging of the internal microstructure of tissues including, but not limited to, the identification of cells, vessels and their organization or architecture.
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
18 Years and over
Who
All
Number of participants
5,000
Started
2026-03-04
Last checked
2026-03

Plain English Summary

What is this study?

  • • Testing a new treatment for adult patients undergoing a surgery or a medical procedure with use of histolog® scanner
  • • Clinical study - 5,000 participants
  • • 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

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with adult patients undergoing a surgery or a medical procedure with use of histolog® scanner

Where?

  • • Guildford - Royal Surrey County Hospital NHS Foundation Trust

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

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.

Adult Patients Undergoing a Surgery or a Medical Procedure With Use of Histolog® ScannerWhatever the Disease Area

How this trial compares with your answers

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What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Age ≥18 years old at the time of consenting
  • ✓Undergoing a surgery or a medical procedure with use of Histolog® Scanner
  • ✓Ability to understand and the willingness to sign a written agreement to take part.

Who cannot take part

  • ✗Active participation in a drug, device, or other medical intervention study that has not reached its primary...
  • ✗Patients under judicial protection, legal guardianship or curatorship.
See the full criteria
Inclusion Criteria: * Age ≥18 years old at the time of consenting * Undergoing a surgery or a medical procedure with use of Histolog® Scanner * Ability to understand and the willingness to sign a written informed consent. Exclusion Criteria: * 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.

Where Is This Study? (1 UK site)

Royal Surrey County Hospital NHS Foundation Trust

Guildford GU2 7XX, United Kingdom

Recruiting
Site contact (verified)
Wissam Abou-ChedidPrincipal Investigator
Consultant Urological Surgeon+44 14 835 711 22w.abouchedid@nhs.net
Data sourced from ClinicalTrials.gov · Last verified: 2026-03