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This is an observational, single-center, open-label photography evaluation. Any patient that arrives for consultation or treatment at the clinic, presenting the required lesions detailed in the protocol can be included.
Full description
This is an observational, single-center, open-label photography evaluation. Any patient that arrives for consultation or treatment at the clinic, presenting the required lesions detailed in the protocol can be included.
The specified lesions can be located on any area of the face or body. For consenting subjects at least 5 close-up images of at least one lesion and one reference image (e.g., subject's skin without any lesion) will be obtained using the Multi-spectral SMART camera. An additional reference image of the lesion area will be taken with a regular camera. Optional images may be taken using a dermatoscop
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Inclusion criteria
Subjects must meet all the following inclusion criteria to be entered into the study:
Any patient, male or female of at least 18 years old, who is willing to sign an informed consent form and present at least one of the following conditions:
Exclusion criteria
Any of the following will exclude the subject from the study:
The study is intended to gather image data so, any patient can be included in the study, and no exclusion criteria apply.
Primary purpose
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Interventional model
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210 participants in 1 patient group
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Central trial contact
Rula Masoud, PhD; Michael Ziv, MD
Data sourced from clinicaltrials.gov
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