Melanin Index in Those With Fitzpatrick Skin Phototypes I-VI

Sponsor
Northwestern University (Other)
Overall Status
Completed
CT.gov ID
NCT01124513
Collaborator
(none)
270
1
3
7
38.4

Study Details

Study Description

Brief Summary

The "gold standard" method of assessing skin pigmentation is spectrophotometry; however, even as early as 1961 the potential for confounding by dilatation of blood vessels was recognized. (Monash 1961) Manual compression was used to express the blood from the field being measured. The red reflectance captured by reflectance spectrophotometer introduced an uncontrollable variable when measuring the tanning /pigmentation response of skin tone/color. Room temperature induced increased or decreased blood flow through the skin, which altered the findings by spectrophotometer. Other potentially confounding variables that changed blood flow were: recent exercise, and the flushing/blushing for emotional reasons. Since these conditions were difficult to reliably control on the sun exposed extremities, spectrophotometry was not a practical method to assess change in melanin over time as an outcome measure for efficacy of sun protection.

Digital imaging with videodermatoscopy utilizing a portable device that is supported by a laptop computer, provides a high resolution digital image for analysis. (EasyScan) As described by Yamamoto et al (2008), applying the Image J freeware to quantify the pigmentation in the digital image holds promise as a practical objective method to reliably assess skin tones based on the melanin content in a non invasive manner. With standardization, the software and hardware may quantify the constitutive pigment in the sun protected skin as the melanin index.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Induced Erythema
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
270 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Screening
Official Title:
A Prospective Study of Melanin Index in Those With Fitzpatrick Skin Phototypes I-VI
Study Start Date :
May 1, 2010
Actual Primary Completion Date :
Dec 1, 2010
Actual Study Completion Date :
Dec 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Digital Camera

Digital camera images will be taken of a a 2cm^2 area of sun protected skin.

Procedure: Induced Erythema
Study personnel will induce erythema by sequentially applying ice for approximately 2 minutes to the 2 cm^2 target region of the upper volar arm. This erythema is a reaction to the vasoconstriction caused by skin cooling. The vasoconstriction is visually monitored to determine the onset of the vascular dilation that occurs after cessation of cooling. Images with the Digital Camera, Spectrophotometer and Videodermoscope are re-taken.

Active Comparator: Spectrophotometer

The probe of the protable reflectance spectrophotometer is lightly applied to the sufance of the skin and a reading is taken.

Procedure: Induced Erythema
Study personnel will induce erythema by sequentially applying ice for approximately 2 minutes to the 2 cm^2 target region of the upper volar arm. This erythema is a reaction to the vasoconstriction caused by skin cooling. The vasoconstriction is visually monitored to determine the onset of the vascular dilation that occurs after cessation of cooling. Images with the Digital Camera, Spectrophotometer and Videodermoscope are re-taken.

Active Comparator: Videodermoscopy

The instrument is put in contact with sun protected skin and an image is taken of a 2 cm^2 area.

Procedure: Induced Erythema
Study personnel will induce erythema by sequentially applying ice for approximately 2 minutes to the 2 cm^2 target region of the upper volar arm. This erythema is a reaction to the vasoconstriction caused by skin cooling. The vasoconstriction is visually monitored to determine the onset of the vascular dilation that occurs after cessation of cooling. Images with the Digital Camera, Spectrophotometer and Videodermoscope are re-taken.

Outcome Measures

Primary Outcome Measures

  1. Change in Melanin Index [2 minutes]

    Compare the MI obtained by the digital camera, videodermoscope and spectrophotmetry between the usual conditions and after the induction of erythema.

  2. Change in Melanin Index for 3 methods (digital camera, videodermoscope and spectrophotmetry) vs. patient-reported skin type vs. dermatologist-determined skin type [Up to 10 minutes]

    Correlate the melanin index under usual conditions by each of the 3 methods (digital camera, videodermoscope and spectrophotometry) with the Fitzpatrick skin phyototype as determined by the patients' responses to standard questions, and the dermatologist's determination of skin type.

  3. Difference in Time to Complete each of the 3 methods (digital camera, videodermoscope and spectrophotometer) [Up to 10 minutes]

    Compare the time of testing (duration of each test for thes ubject, time spent by the research assistant administering the test) between the digitical camera, videodermoscope and spectrophotometer.

  4. Desirability and Relevance of Videodermoscopy Image [Up to 10 minutes]

    Assess desirability and relevance of the image obtained by videodermoscopy to the subject especially with reference to the subject's assessment of their risk of sunburning.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 89 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • at least 18 years old

  • fluent in English

  • able to complete the study procedures including answering questionnairs

  • willing to apply ice to left upper inner arm

  • willing to have digital photos, dermatoscopic photos and spectrophometry readings taken of left upper inner arm

Exclusion Criteria:
  • have a history of vitiligo or currently has vitiligo

  • use self-tanning products or tan accelerators ont he left upper inner arm int he 4 weeks prior to enrollment

  • history of cold urticaria or conenctive tissue disease such as scleroderma

Contacts and Locations

Locations

Site City State Country Postal Code
1 Northwestern University Chicago Illinois United States 60611

Sponsors and Collaborators

  • Northwestern University

Investigators

  • Principal Investigator: June K Robinson, MD, Northwestern University
  • Study Director: Dennis P West, PhD, Northwestern University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
June Robinson, Professor of Dermatology, Northwestern University
ClinicalTrials.gov Identifier:
NCT01124513
Other Study ID Numbers:
  • JR-STU27549
First Posted:
May 17, 2010
Last Update Posted:
Mar 18, 2015
Last Verified:
Mar 1, 2015
Keywords provided by June Robinson, Professor of Dermatology, Northwestern University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 18, 2015