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NCT04705168

Study of the Nevisense Device to Assess Atypical Skin Lesions

Completed Last updated 20 November 2025
What this trial tests

trial testing Nevisense electrical impedance spectroscopy in Nevus in 40 participants. Completed in 18 November 2025.

Timeline
8 January 2021
Primary endpoint
18 November 2025
18 November 2025

Quick facts

Lead sponsorMemorial Sloan Kettering Cancer Center
StatusCompleted
Study typeOBSERVATIONAL
Enrollment40
Start date8 January 2021
Primary completion18 November 2025
Estimated completion18 November 2025
Sites3 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Memorial Sloan Kettering Cancer Center — full company profile →

Who can join

30 and older, any sex, with Nevus or Multiple Nevi. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to find out whether the Nevisense device can provide useful information about atypical moles to complement the usual assessments done during routine screening for melanoma. Assessing particpants' moles with the Nevisense device may help improve screening methods for the early detection of melanoma in people with atypical mole syndrome.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Memorial Sloan Kettering Cancer Center trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04705168.

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