Avene Compact Honey for Prevention of Pigmentation From Visible Light

Healthy Clinical Trial

Official title: A Randomized, Single-blind Study of the Ability of Avène Compact Honey to Prevent Pigmentation Induced by Visible Light in Subjects With Skin Phototype III or IV

Status Completed

Clinical Trial Summary

The main objective of the study is to assess the efficacy of Avène Compact Honey in preventing pigmentation induced by visible light in subjects with a phototype III or IV.

Patients will be exposed to a range of visible light to areas on the back to confirm study eligibility. Patients showing pigmentation after 7 days on the exposed areas will be eligible to continue.

Eligible patients will have study product applied to part of the back. The back will be exposed to a range of light based on the minimum exposure inducing pigmentation previously ascertained. The area where study product is applied will have a higher range of light exposure than the area without the study product.

Seven days later, the areas will be examined to determine the lowest exposure inducing pigmentation on the sides with and without study product. The color will also be measured between two identical exposures with and without the applied study product.

Clinical Trial Description

Part A At Day -7, all subjects will be exposed to a range of doses of visible light on an approximately 0.90 cm diameter area on the back to ascertain their predisposition for pigmentation induced by visible light. The doses will be 30, 40, 60, 80, 100 and 120 J cm-2. At the Day 0 visit, subjects' pigmentation will be determined by investigator visual assessment. Subjects with a lowest observed pigmentation at the 30 J cm-2 or the 120 J cm-2 dose will not continue in the study. For each subject that continues, the area where Avène Compact Honey will be applied on the back will be randomized. At least 15 minutes later, unprotected areas will be exposed to doses ranging from ~1/20th to 1.8 times the lowest dose of visible light that induced pigmentation at Day -7. To not unnecessarily over expose subjects, the first 3 will have protected areas exposed to doses ranging from ~half to 16 times the lowest dose of visible light that induced pigmentation at Day -7. All subjects will have an additional exposure on the protected side equal to the highest dose of the unprotected side for colorimetric comparison. Subjects will be examined at Day 7 (seven days after visible light exposure). Pigmentation on all exposed areas will be evaluated by investigator visual assessment. The colorimetric measurements on protected and unprotected skin will be recorded for the equivalent exposures and for adjacent skin. The exposed area on the protected side to be tested with colorimetric analysis will be hidden during the investigator visual assessment. The minimum dose on the unprotected side and an area of unprotected and unexposed skin will be hidden from the colorimetric evaluator to maintain the blind. The lowest visible light dose inducing pigmentation will be recorded for both the unprotected and protected areas. If the first three subjects are only pigmented at either the 16X level or not at all on the protected side, then the remaining subjects in the study will be exposed at doses ranging from 0.7 to as high as 24 times the lowest dose of visible light that induced pigmentation at Day -7.

Part B At Day 0, all subjects will be exposed to a range of doses of visible light on an approximately 0.90 cm diameter area on the back to ascertain their disposition for pigmentation induced by visible light. The doses will be 8, 40, 80, 160, 320 and 480 J cm-2. At the Day 7 visit, subjects' pigmentation will be determined by investigator visual assessment. Subjects will be divided into 2 cohorts. Cohort A will contain 5 subjects of phototype IV with dark skin and cohort B will contain 5 subjects with skin phototype V.

Part C At Day -7, all subjects will be exposed to a range of doses of visible light on an approximately 0.90 cm diameter area on the back to ascertain their predisposition for pigmentation induced by visible light. The doses will be 8, 40, 80, 160, 320 and 480 J cm-2. At the Day 0 visit, subjects' pigmentation will be determined by investigator visual assessment. Subjects with a lowest observed pigmentation at the 8 J cm-2 dose will not continue in the study and neither will subjects showing no pigmentation at 480 J cm-2. For each subject that continues, the area where Avène Compact Honey will be applied on the back will be randomized and then receive the application. At least 15 minutes later, protected areas will be exposed to doses of 32, 160, 320, 640, 1280 and 1920 cm-2. Unprotected areas will be exposed to the same doses as Day 0. To not unnecessarily over expose subjects, those with a lowest observed pigmentation at Day 0 of 40 or 80 J cm-2 will have the maximum exposure at Day 0 determined at the investigators discretion. Subjects will be examined at Day 7 (seven days after visible light exposure). Pigmentation on all exposed areas will be evaluated by investigator visual assessment. The lowest visible light dose inducing pigmentation will be recorded for both the unprotected and protected areas. The colorimetric measurements on protected and unprotected skin will be recorded for the equivalent exposures and for adjacent skin. Four areas of unprotected and protected skin will be hidden from the colorimetric evaluator to maintain the blind. Subjects will be divided into 2 cohorts. Cohort A will contain 5 subjects of phototype IV with dark skin and cohort B will contain 5 subjects with skin phototype V. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Healthy

• NCT number: NCT01448122
• Study type: Interventional
• Source: Pierre Fabre Dermo Cosmetique
• Status: Completed
• Phase: N/A
• Start date: October 2011
• Completion date: December 2012