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Clinical Trial of 4% Niacinamide Versus 0.05% Desonide for the Treatment of Axillar Hyperpigmentation

Primary Purpose

Hyperpigmentation

Status
Completed
Phase
Phase 4
Locations
Mexico
Study Type
Interventional
Intervention
Desonide
Niacinamide
Placebo
Sponsored by
Universidad Autonoma de San Luis Potosí
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hyperpigmentation focused on measuring Inflammatory hyperpigmentation, axillar pigmentation

Eligibility Criteria

18 Years - 50 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Women over 18 years old
  • Healthy
  • Clinical diagnosis of axillar hyperpigmentation

Exclusion Criteria:

  • Pregnancy or lactation
  • Obesity
  • Endocrinological diseases
  • Mental diseases
  • Treatment for axillar hyperpigmentation in the last 2 months

Sites / Locations

  • Dermatology Department. Hospital Central "Dr. Ignacio Morones Prieto"

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

Niacinamide

Desonide

Placebo

Arm Description

4% niacinamide cream that will be randomly applied on axillar hyperpigmentation once-a-day for 9 weeks.

Once-a-day application of 0.05% desonide cream on axillar hyperpigmentation

Humectant placebo cream

Outcomes

Primary Outcome Measures

Pigmentation
Quantification of melanin content in histologic sections by Fontana-Masson stain

Secondary Outcome Measures

Inflammation
Quantification of inflammatory infiltrate in skin biopsies by histologic lymphocites infiltrate and immunohistochemistry stain anti-CD1
Trauma
To detect trauma we measure damage in Membrane Basal by anti-collagen IV immunohistochemistry stain
Change in transepidermal water loss in hyperpigmented lesion
Quantification of water loss measured by a evaporimeter in grams per squared meter per hour. Is an indirect measure of inflammation.
Investigator's Depigmentation Improvement
Clinical improvement is assessed by means of digital photographic registration (frontal, right, and left views). Two independent observers clinically graded the global improvement as poor (0-25%), mild (26-50%), good (51-75%), and excellent (>75%).

Full Information

First Posted
February 21, 2012
Last Updated
November 27, 2012
Sponsor
Universidad Autonoma de San Luis Potosí
Collaborators
Hospital Central "Dr. Ignacio Morones Prieto"
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1. Study Identification

Unique Protocol Identification Number
NCT01542138
Brief Title
Clinical Trial of 4% Niacinamide Versus 0.05% Desonide for the Treatment of Axillar Hyperpigmentation
Official Title
A Double Blind, Randomized Clinical Trial of 4% Niacinamide Versus 0.05% Desonide for the Treatment of Axillar Hyperpigmentation
Study Type
Interventional

2. Study Status

Record Verification Date
November 2012
Overall Recruitment Status
Completed
Study Start Date
July 2011 (undefined)
Primary Completion Date
November 2012 (Actual)
Study Completion Date
November 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidad Autonoma de San Luis Potosí
Collaborators
Hospital Central "Dr. Ignacio Morones Prieto"

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Axillary hyperpigmentation is a frequent consultation in dark skin populations although its exact prevalency is unknown. Currently, there are not studies about physiopathology and treatment for this entity. The objective is to evaluate the depigmenting effect of topical 4% niacinamide versus 0.05% desonide in axillary hyperpigmentation. At least 30 axillas with hyperpigmentation in individuals of phototype III-V, aged 18-50 years are going to be randomly assigned to receive niacinamide, desonide or placebo daily. No hygienic habits will not be modified. Volunteers will be evaluated at baseline and for 9 weeks, by means of histological, histochemical and immunohistochemistry analysis, as well as Transepidermal Water Loss (TEWL), colorimetry, clinically and by photography control.
Detailed Description
Axillary hyperpigmentation is frequent in dark skin population, is possible a type of postinflammatory hyperpigmentation present in phototypes IV to VI. Previous reports have described increased intensity of Masson-Fontana, anti-tyrosinase and/or anti-TRP1 staining, indicative of melanocyte stimulation and increased melanin production, but the exact mechanism is unknown. The hair plucking, the rubbing of clothes on skin and physical stimulation from washing and drying the underarm are factors implicated. The objective of our study is evaluate the depigmenting effect of topical niacinamide versus desonide in axillary hyperpigmentation through the histochemistry and immunohistochemistry staining. The study population will include at least 30 axillas with hyperpigmentation in a population with phototype III-V and aged 18-50 years old. Informed consent will be obtained from the patients, under approval by the local ethical committee (Institutional Review Board). The patients are going to be randomly assigned to receive 4% niacinamide, 0.05% desonide or placebo daily once at night. None hygienic habit is going to be modified. Volunteers will be evaluated at baseline and 9 weeks later, with histochemical and immunohistochemical analysis (biopsies), colorimetric value axis L*, a*, b* (Chromameter CR-300, Minolta, Osaka, Japan), Transepidermal Water Loss (TEWL) by means of an evaporimeter (Dermalab, Cortex Technology, Denmark), clinical assessment and photography control. Statistical analysis was performed using t student, the level of significance was set at 5%. And clinical evaluation will be analysed by means of chi square test.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hyperpigmentation
Keywords
Inflammatory hyperpigmentation, axillar pigmentation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
28 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Niacinamide
Arm Type
Active Comparator
Arm Description
4% niacinamide cream that will be randomly applied on axillar hyperpigmentation once-a-day for 9 weeks.
Arm Title
Desonide
Arm Type
Active Comparator
Arm Description
Once-a-day application of 0.05% desonide cream on axillar hyperpigmentation
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Humectant placebo cream
Intervention Type
Drug
Intervention Name(s)
Desonide
Other Intervention Name(s)
0.05% Desowen cream, Galderma, France.
Intervention Description
Once-a-day applying on axillar hyperpigmentation for 9 weeks
Intervention Type
Drug
Intervention Name(s)
Niacinamide
Other Intervention Name(s)
Nicotinamide, nicomide
Intervention Description
Once-a-day applying on axillar hyperpigmentation for 9 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
vanicream, cetaphil
Intervention Description
Humectant placebo cream
Primary Outcome Measure Information:
Title
Pigmentation
Description
Quantification of melanin content in histologic sections by Fontana-Masson stain
Time Frame
9 weeks
Secondary Outcome Measure Information:
Title
Inflammation
Description
Quantification of inflammatory infiltrate in skin biopsies by histologic lymphocites infiltrate and immunohistochemistry stain anti-CD1
Time Frame
9 weeks
Title
Trauma
Description
To detect trauma we measure damage in Membrane Basal by anti-collagen IV immunohistochemistry stain
Time Frame
9 weeks
Title
Change in transepidermal water loss in hyperpigmented lesion
Description
Quantification of water loss measured by a evaporimeter in grams per squared meter per hour. Is an indirect measure of inflammation.
Time Frame
9 weeks
Title
Investigator's Depigmentation Improvement
Description
Clinical improvement is assessed by means of digital photographic registration (frontal, right, and left views). Two independent observers clinically graded the global improvement as poor (0-25%), mild (26-50%), good (51-75%), and excellent (>75%).
Time Frame
9 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Women over 18 years old Healthy Clinical diagnosis of axillar hyperpigmentation Exclusion Criteria: Pregnancy or lactation Obesity Endocrinological diseases Mental diseases Treatment for axillar hyperpigmentation in the last 2 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bertha Torres-Alvarez, MD
Organizational Affiliation
Dermatology Department. Hospital Central "Dr. Ignacio Morones Prieto", San Luis Potosi, México
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Gabryela N Larraga-Piñones, MD
Organizational Affiliation
Dermatology Department. Hospital Central "Dr. Ignacio Morones Prieto". San Luis Potosi, México
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Juan P Castanedo-Cázares, MD
Organizational Affiliation
Dermatology Department. Hospital Central "Dr. Ignacio Morones Prieto". San Luis Potosi, México
Official's Role
Study Director
Facility Information:
Facility Name
Dermatology Department. Hospital Central "Dr. Ignacio Morones Prieto"
City
San Luis Potosi
ZIP/Postal Code
78210
Country
Mexico

12. IPD Sharing Statement

Citations:
PubMed Identifier
21822427
Citation
Navarrete-Solis J, Castanedo-Cazares JP, Torres-Alvarez B, Oros-Ovalle C, Fuentes-Ahumada C, Gonzalez FJ, Martinez-Ramirez JD, Moncada B. A Double-Blind, Randomized Clinical Trial of Niacinamide 4% versus Hydroquinone 4% in the Treatment of Melasma. Dermatol Res Pract. 2011;2011:379173. doi: 10.1155/2011/379173. Epub 2011 Jul 21.
Results Reference
background
PubMed Identifier
21317614
Citation
Torres-Alvarez B, Mesa-Garza IG, Castanedo-Cazares JP, Fuentes-Ahumada C, Oros-Ovalle C, Navarrete-Solis J, Moncada B. Histochemical and immunohistochemical study in melasma: evidence of damage in the basal membrane. Am J Dermatopathol. 2011 May;33(3):291-5. doi: 10.1097/DAD.0b013e3181ef2d45.
Results Reference
background

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Clinical Trial of 4% Niacinamide Versus 0.05% Desonide for the Treatment of Axillar Hyperpigmentation

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