EU Post-Market Registry to Collect Real-World Clinical Data on the Use of the Histolog Scanner.
Recruiting
Observational Study
Adult Patients Undergoing a Surgery or a Medical Procedure With Use of Histolog® Scanner
Whatever the Disease Area
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 5,000 (estimated)
- Sponsor
- SamanTree Medical SA · Industry
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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.
Trial Locations
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Eligibility 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 medi…
Contacts
No contact information available.