A Study of Noninvasive Methods to Evaluate Skin and Mucosal Conditions

Description

The purpose of this study is to find out whether using noninvasive methods to study the appearance of lesions can improve diagnostic accuracy before a biopsy is required and help guide treatment planning. The database created to store these images is called an Image Repository, and it will be used to support clinical practice, teaching and training, and future research.The High-resolution OCT (Apollo Medical Optics) device ApolloVue® S100 Image System (medical device Class II) can provide both cross-sectional and en-face images with cellular information.

Conditions

Skin Lesion, Mucosal Lesion

Study Overview

Study Details

Study overview

The purpose of this study is to find out whether using noninvasive methods to study the appearance of lesions can improve diagnostic accuracy before a biopsy is required and help guide treatment planning. The database created to store these images is called an Image Repository, and it will be used to support clinical practice, teaching and training, and future research.The High-resolution OCT (Apollo Medical Optics) device ApolloVue® S100 Image System (medical device Class II) can provide both cross-sectional and en-face images with cellular information.

Noninvasive Assessment of Muco-cutaneous Lesions In Vivo

A Study of Noninvasive Methods to Evaluate Skin and Mucosal Conditions

Condition
Skin Lesion
Intervention / Treatment

-

Contacts and Locations

New York

Memorial Sloan Kettering Cancer Center (All Protocol Activities), New York, New York, United States, 10065

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * All ages
  • * Patients with a muco-cutaneous lesion(s) amenable to imaging by non-invasive tools
  • * Healthy volunteer subjects
  • * Ability to give informed consent or in the case of pediatric patients, assent and consent from the parent/guardian
  • * Allergy or intolerance to ultrasound gel or mineral oil used for imaging
  • * Patients who are not able to comply with imaging procedure

Ages Eligible for Study

to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Memorial Sloan Kettering Cancer Center,

Manu Jain, MD, PRINCIPAL_INVESTIGATOR, Memorial Sloan Kettering Cancer Center

Study Record Dates

2031-08-02