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Clinical Trials/NCT00764920
NCT00764920
Active, not recruiting
Not Applicable

Non-invasive Imaging Modalities for Assessment of Normal and Lesional Skin

University of California, Irvine1 site in 1 country750 target enrollmentOctober 1, 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pigmented Skin Lesion of Uncertain Nature
Sponsor
University of California, Irvine
Enrollment
750
Locations
1
Primary Endpoint
Collect information on normal and lesional skin
Status
Active, not recruiting
Last Updated
9 months ago

Overview

Brief Summary

The purpose of this research is to develop non-invasive imaging modalities for assessment of skin. This is a pilot study which will use multiple imaging modalities to collect information on normal and lesional skin. The researchers understand that the purpose of this study is not to evaluate any particular treatment and an investigation of a new therapeutic intervention would require an additional protocol. Skin conditions to be studied include vascular lesions, pigmentary disorders, inflammatory conditions and neoplasms.

Detailed Description

Normal and lesional skin will be assessed by the following imaging modalities: 1. Laser Speckle Imaging can provide information about relative blood flow in a tissue. In skin it can be used to determine what areas have more blood flow and whether a particular intervention or treatment affects blood flow. 2. Optical Coherence Tomography and Optical Doppler Tomography can provide pictures of blood vessels in an area of the body and can also tell how fast blood is flowing in that area. 3. Photon Migration Spectroscopy can provide information about the amount of blood, oxygen, fat and water is in a tissue. 4. Multi-Spectral Imaging can provide a 3 dimensional image of structures within the skin. 5. Multiphoton Microscopy can provide images of structures of the skin.

Registry
clinicaltrials.gov
Start Date
October 1, 2008
End Date
December 1, 2026
Last Updated
9 months ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kristen Kelly

Professor Departments of Dermatology and Surgery

University of California, Irvine

Eligibility Criteria

Inclusion Criteria

  • adult male or female 7 and older; able to carry out study instructions

Exclusion Criteria

  • Younger than 7 years old
  • pregnant woman
  • breast feeding

Outcomes

Primary Outcomes

Collect information on normal and lesional skin

Time Frame: up to 12 weeks

Develop non-invasive imaging modalities for assessment of skin.

Study Sites (1)

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