Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06666790

DermaSensor Postmarket Surveillance Study

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
396 (estimated)
Sponsor
DermaSensor, Inc. · Industry
Sex
All
Age
40 Years
Healthy volunteers
Not accepted

Summary

The objective of this study is to evaluate the sensitivity of the DermaSensor device and Investigators when used on skin lesions concerning for melanoma.

Conditions

Interventions

TypeNameDescription
DEVICEScan with elastic scattering spectroscopy device to assess risk of malignancyElastic scattering spectroscopy device uses a spectrum of light reflectance to compare suspicious lesion signature to that of previously scanned lesions with known benign or malignant pathology

Timeline

Start date
2024-10-08
Primary completion
2027-04-11
Completion
2027-09-10
First posted
2024-10-31
Last updated
2024-10-31

Locations

2 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT06666790. Inclusion in this directory is not an endorsement.

DermaSensor Postmarket Surveillance Study (NCT06666790) · Clinical Trials Directory