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NCT01118832

Using High Resolution Function Imaging To Detect Melanoma and Dysplastic Nevi

Completed Last updated 8 February 2019
What this trial tests

trial in Melanoma in 30 participants. Completed in 20 February 2012.

Timeline
22 September 2009
Primary endpoint
29 June 2010
20 February 2012

Quick facts

Lead sponsorSidney Kimmel Comprehensive Cancer Center at Johns Hopkins
StatusCompleted
Study typeOBSERVATIONAL
Enrollment30
Start date22 September 2009
Primary completion29 June 2010
Estimated completion20 February 2012
Sites1 location across United States

Conditions studied

Sponsor

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins — full company profile →

Who can join

Adults 10 to 80, any sex, with Melanoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A novel infrared imaging tool to aid in the clinical detection of atypical pigmented lesions and melanoma is developed. Goals include evaluation of the utility of high-resolution infrared scanning of cutaneous lesions in the diagnosis of pigmented lesions and the identification of high-risk lesions and melanomas.

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 recruiting trials for Melanoma

Currently open trials in the same condition.

Other Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins 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/NCT01118832.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing