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ID04743362

Noninvasive Imaging Evaluation of Skin and Mucosal Lesions Using Advanced Diagnostic Technologies to Support Care and Research

Led by Memorial Sloan Kettering Cancer Center · Updated on 2026-04-23

5010

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating noninvasive imaging methods to study the appearance of skin and mucosal lesions to improve diagnostic accuracy before a biopsy is needed and to help guide treatment planning. This study involves creating an Image Repository to store these images for clinical practice, teaching, training, and future research. It uses a high-resolution Optical Coherence Tomography OCT device called ApolloVueae S100 Image System that provides detailed cross-sectional and en-face images with cellular information. Participants with muco-cutaneous lesions, including normal skin, benign lesions, or neoplastic conditions, identified during routine clinical care will undergo various non-invasive imaging tests. These include dermoscopic imaging, 3-dimensional total body photography, confocal microscopy, OCT imaging, ultrasound, hyperspectral imaging, electrical impedance spectroscopy, and patient self-imaging using mobile phone technology with dermatoscope attachments. Images will be collected of untreated and treated lesions over a period of 7 years. Participants will have their lesions imaged using these non-invasive tools, with images collected and stored in the Image Repository. Assessments include capturing detailed images using specialized devices to evaluate lesion morphology, depth, vascular features, and biochemical information. Researchers will monitor the imaging data to support clinical decisions, teaching, and future research. Participation may involve multiple imaging sessions over time, and safety monitoring includes ensuring no allergic reactions to imaging materials. The study welcomes healthy volunteers and all ages, with informed consent or parental consent and patient assent as applicable.

CONDITIONS

Brief Title

A Study of Noninvasive Methods to Evaluate Skin and Mucosal Conditions

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients of all ages
  • Patients with muco-cutaneous lesion(s) that can be imaged by non-invasive tools
  • Healthy volunteer subjects
  • Ability to give informed consent or, for pediatric patients, assent and parental/guardian consent
Not Eligible

You will not qualify if you...

  • Allergy or intolerance to ultrasound gel or mineral oil used during imaging
  • Inability to comply with imaging procedures

Research Team

M

Manu Jain, MD

V

Veronica Rotemberg, MD

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