DermaSensor Postmarket Surveillance Study for Melanoma

This study is testing a device called DermaSensor to see how well it can identify skin lesions that might be melanoma. The DermaSensor device uses light to compare suspicious spots on your skin to known benign (non-cancerous) or malignant (cancerous) lesions. We are looking for men and women aged 40 and older who have a skin lesion that their doctor thinks might be melanoma. The main goal is to see how accurate the DermaSensor device is at detecting melanoma. The study is currently unclear on its recruitment status and plans to enroll 396 participants.

Study design
This is an interventional study that plans to enroll 396 participants. It is evaluating a device rather than a drug.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
The device's sensitivity will be measured at 39 months, suggesting a follow-up period.

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NCT06666790

DermaSensor Postmarket Surveillance Study

Recruiting
NAAges 40+InterventionalScreening
DermaSensor, Inc.
~396 participants
Updated 2024-10-31 on ClinicalTrials.gov
What's tested:Scan with elastic scattering spectroscopy device to assess risk of malignancy

At a glance

Recruiting sites
2 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Device Sensitivity
Measured over 39 months
Melanoma, Skin
2 sites across 2 states
Florida1
North Carolina1
  • Gary Slatko, MD, MBA · STUDY_CHAIR · DermaSensor, Inc.

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  • Device Sensitivity39 months