Viewing Study NCT04705168


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Ignite Modification Date: 2026-01-02 @ 5:27 AM
Study NCT ID: NCT04705168
Status: COMPLETED
Last Update Posted: 2025-11-20
First Post: 2021-01-08
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: Study of the Nevisense Device to Assess Atypical Skin Lesions
Sponsor: Memorial Sloan Kettering Cancer Center
Organization:

Study Overview

Official Title: Performance of Nevisense Electrical Impedance Spectroscopy in Patients With Multiple Nevi and Large Acquired Nevi (LAN)
Status: COMPLETED
Status Verified Date: 2025-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: 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.
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: