AI-Powered dermatoscope aims to spot skin cancer faster
NCT ID NCT03818620
First seen Oct 05, 2026 · Last updated Oct 06, 2026 · Updated 1 time
Summary
Researchers are testing a new digital dermatoscope called DermScan that uses automatic decision support to help identify skin cancer. The study enrolls adults with skin lesions and collects images with both the new device and a standard dermatoscope. The goal is to build a large database of anonymized images and compare how well the new device performs against standard care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Barco digital dermatoscope device
- What this could lead to
- If the device works well, it could help doctors detect skin cancer earlier and make dermatology exams more efficient.
- What could go wrong
- The device may not perform better than standard dermoscopy, and the AI algorithms need large, diverse datasets to work reliably. This observational study does not test whether the device improves patient outcomes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
4,339 people
The number who actually took part.
- Started
-
Jun 2017
- Finished
-
May 2025
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients will be considered for enrollment in the study when they have a lesion that is accessible to the Barco Digital Dermatoscope, are able to give informed consent and are over 18 years old.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * The patient has a lesion that is accessible to the Barco Digital Dermatoscope * Patient gives informed consent * Men or women of any ethnic group aged ≥ 18 years Exclusion Criteria: * Men or women of any ethnic group aged \< 18 years * Patients not willing or able to read, understand and sign the study-specific informed consent form
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
UZ / KU Leuven
Leuven, 3000, Belgium
-
UZ Gent
Ghent, 9000, Belgium
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Other studies related to the condition(s) this trial covers.
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