Clinical Trial of 4% Niacinamide Versus 0.05% Desonide for the Treatment of Axillar Hyperpigmentation
Information source: Universidad Autonoma de San Luis Potosí
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Hyperpigmentation
Intervention: Desonide (Drug); Niacinamide (Drug); Placebo (Drug)
Phase: Phase 4
Status: Completed
Sponsored by: Universidad Autonoma de San Luis Potosí Official(s) and/or principal investigator(s): Bertha Torres-Alvarez, MD, Study Chair, Affiliation: Dermatology Department. Hospital Central "Dr. Ignacio Morones Prieto", San Luis Potosi, México Gabryela N Larraga-Piñones, MD, Principal Investigator, Affiliation: Dermatology Department. Hospital Central "Dr. Ignacio Morones Prieto". San Luis Potosi, México Juan P Castanedo-Cázares, MD, Study Director, Affiliation: Dermatology Department. Hospital Central "Dr. Ignacio Morones Prieto". San Luis Potosi, México
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.
Clinical Details
Official title: A Double Blind, Randomized Clinical Trial of 4% Niacinamide Versus 0.05% Desonide for the Treatment of Axillar Hyperpigmentation
Study design: Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Primary outcome: Pigmentation
Secondary outcome: InflammationTrauma Change in transepidermal water loss in hyperpigmented lesion Investigator's Depigmentation Improvement
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.
Eligibility
Minimum age: 18 Years.
Maximum age: 50 Years.
Gender(s): Female.
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
Locations and Contacts
Dermatology Department. Hospital Central "Dr. Ignacio Morones Prieto", San Luis Potosi 78210, Mexico
Additional Information
Related publications: Navarrete-SolÃs J, Castanedo-Cázares JP, Torres-Ãlvarez B, Oros-Ovalle C, Fuentes-Ahumada C, González FJ, MartÃnez-RamÃrez 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. Torres-Ãlvarez B, Mesa-Garza IG, Castanedo-Cázares 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.
Starting date: July 2011
Last updated: November 27, 2012
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