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Clinical Trial of Hydroquinone Versus Miconazol in Melasma

Primary Purpose

Melasma

Status
Unknown status
Phase
Phase 4
Locations
Mexico
Study Type
Interventional
Intervention
Miconazole
Hydroquinone
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 Melasma focused on measuring Melasma, miconazole, hydroquinone

Eligibility Criteria

18 Years - 60 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Signed informed consent
  • Mexican women over 18 years of age
  • Dermatologic diagnostic of melasma
  • Phototype III or more

Exclusion Criteria:

  • Pregnant or breastfeeding
  • Postbirth, abortion in the past 6 months
  • Having an endocrine or autoimmune disease
  • Under hormonal therapy of any kind including contraceptives or it´s use in the past 6 months
  • Currently under treatment for melasma including sunblock
  • Currently under radiation therapy, chemotherapy, immunosuppressants of any kind or phototherapy or it´s use in the past 6 months
  • Having used or are consuming photosensitizing substances, oral or topical

Sites / Locations

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

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Placebo Comparator

Arm Label

Miconazole

Hydroquinone

Placebo

Arm Description

OTC topical prescription used for fungal treatment that can be useful to the treatment of melasma due to its depigmenting properties.

Hydroquinone 4% cream (Topical use) a depigmenting agent used as reference will be used as control. It will be applied twice a day for 9 weeks.

Moisturizer cream without pharmacological effects will be used as a control.

Outcomes

Primary Outcome Measures

Depigmentation of melasma lesions by Colorimetry
Quantification of the colour change in the melasma lesions by means of the L axis of the CIE system. 0 is pure white, 100 y total dark.

Secondary Outcome Measures

Global Physician Assessment
Clinical improvement is assessed by means of digital photographic registration (frontal, right, and left views). An independent observer clinically graded the global improvement as poor (0-25%), mild (26-50%), good (51-75%), and excellent (>75%).
MASI (Melasma Area Severity Index)
The total score would range from 0-24, involving the forehead (30%), right malar (30%), left malar (30%) and chin (10%), and using area of involvement (0=absent, 1=<10%, 2=10%-29%, 3=30%-49%, 4=50%-69%, 5=70%-89% and 6=90%-100%) and darkness (0=absent, 1=slight, 2=mild, 3=marked and 4=severe). Computation would be as follows: 0.3 A(f) D(f) + 0.3 A(lm) D(lm) + 0.3 A(rm) D(rm) + 0.1 A(c) D(c).
Melanin content by Fontana Masson stain
The Fontana-Masson Stain is specific for melanin, this histochemical reaction reveals accumulations of black material wherever melanin is located. A skin biopsy of lesions will be taken initially and at the end of study. The melanin content will be quantified by a software image analysis of the slides.

Full Information

First Posted
August 7, 2012
Last Updated
December 1, 2014
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
NCT01661556
Brief Title
Clinical Trial of Hydroquinone Versus Miconazol in Melasma
Official Title
Double Blind Randomized Study of 2% Miconazol Versus 4% Hydroquinone in the Treatment for Melasma.
Study Type
Interventional

2. Study Status

Record Verification Date
December 2014
Overall Recruitment Status
Unknown status
Study Start Date
October 2011 (undefined)
Primary Completion Date
February 2015 (Anticipated)
Study Completion Date
December 2015 (Anticipated)

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
Melasma is an acquired discoloration of the skin characterized by brown colour changes commonly on the face.The duration of this double-blind clinical trial will be 12 weeks. The control group will receive treatment with topical Hydroquinone (4%), and the other group topical miconazole. Miconazol has antimelanotic properties and can be used as treatment for melasma patients. The estimated number of subjects to be recruited and randomized for the study is at least 30. The purpose of this study is determine if there is a difference in the effectiveness of these two agents. Melasma Area and Severity Index (MASI) score will be assessed at the beginning of the study and at weeks 4, 8, and 12. Photographs, colorimetry and histological assessment will be also evaluated. Occurrence of adverse effects will also be recorded.
Detailed Description
Melasma is a common acquired hypermelanosis in dark skin populations, usually characterized by symmetrical, irregular macules occurring in photo-exposed areas such as face. Treatment with depigmenting compounds such as hydroquinone, are still the gold standard in this condition. Miconazol has depigmented properties that could be used as part of the treatment in melasma patients. This effect is exerted by inhibiting the tyrosinase enzyme. So, the primary objective of this study is to compare the depigmenting activity of miconazole against hydroquinone. Patients who are included in the study will be randomly assigned to receive one of the treatments, which should use for 12 weeks. The medications should be applied in the affected regions twice a day. The evaluation of clinical improvement will be done in a blinded modality by means of the MASI score, the Global Physician Assessment, as well as colorimetry and histological melanin content. Evaluations will be held on visits at 4, 8 and 12 weeks. Skin biopsy will be taken at onset and at 12 weeks. At the end of the study, data will be compared concerning the former parameters. All side effects will be recorded and analysed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Melasma
Keywords
Melasma, miconazole, hydroquinone

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Miconazole
Arm Type
Experimental
Arm Description
OTC topical prescription used for fungal treatment that can be useful to the treatment of melasma due to its depigmenting properties.
Arm Title
Hydroquinone
Arm Type
Active Comparator
Arm Description
Hydroquinone 4% cream (Topical use) a depigmenting agent used as reference will be used as control. It will be applied twice a day for 9 weeks.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Moisturizer cream without pharmacological effects will be used as a control.
Intervention Type
Drug
Intervention Name(s)
Miconazole
Other Intervention Name(s)
Canesten, Monistat, Micatin
Intervention Description
Miconazole 2% cream will be applied twice a day for 9 weeks. The affected surface will be washed and dried before application with a thin layer of the emulsion as indicated on the affected areas of the face.
Intervention Type
Drug
Intervention Name(s)
Hydroquinone
Other Intervention Name(s)
Eldoquin, Melanex
Intervention Description
Hydroquinone 4% cream (Topical use), will be applied twice a day for 9 weeks. The affected surface will be washed and dried before application with a thin layer of the emulsion on affected areas of the face.
Primary Outcome Measure Information:
Title
Depigmentation of melasma lesions by Colorimetry
Description
Quantification of the colour change in the melasma lesions by means of the L axis of the CIE system. 0 is pure white, 100 y total dark.
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Global Physician Assessment
Description
Clinical improvement is assessed by means of digital photographic registration (frontal, right, and left views). An independent observer clinically graded the global improvement as poor (0-25%), mild (26-50%), good (51-75%), and excellent (>75%).
Time Frame
12 weeks
Title
MASI (Melasma Area Severity Index)
Description
The total score would range from 0-24, involving the forehead (30%), right malar (30%), left malar (30%) and chin (10%), and using area of involvement (0=absent, 1=<10%, 2=10%-29%, 3=30%-49%, 4=50%-69%, 5=70%-89% and 6=90%-100%) and darkness (0=absent, 1=slight, 2=mild, 3=marked and 4=severe). Computation would be as follows: 0.3 A(f) D(f) + 0.3 A(lm) D(lm) + 0.3 A(rm) D(rm) + 0.1 A(c) D(c).
Time Frame
12 weeks
Title
Melanin content by Fontana Masson stain
Description
The Fontana-Masson Stain is specific for melanin, this histochemical reaction reveals accumulations of black material wherever melanin is located. A skin biopsy of lesions will be taken initially and at the end of study. The melanin content will be quantified by a software image analysis of the slides.
Time Frame
12 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Signed informed consent Mexican women over 18 years of age Dermatologic diagnostic of melasma Phototype III or more Exclusion Criteria: Pregnant or breastfeeding Postbirth, abortion in the past 6 months Having an endocrine or autoimmune disease Under hormonal therapy of any kind including contraceptives or it´s use in the past 6 months Currently under treatment for melasma including sunblock Currently under radiation therapy, chemotherapy, immunosuppressants of any kind or phototherapy or it´s use in the past 6 months Having used or are consuming photosensitizing substances, oral or topical
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Amalia Reyes-Herrera, M.D.
Phone
52014448342795
First Name & Middle Initial & Last Name or Official Title & Degree
Juan P Castanedo-Cazares, M.D.
Phone
52014448342795
Email
castanju@yahoo.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juan P Castanedo-Cazares, M.D.
Organizational Affiliation
Hospital Central "Dr. Ignacio Morones Prieto". UASLP
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Amalia Reyes-Herrera, M.D.
Organizational Affiliation
Hospital Central "Dr. Ignacio Morones Prieto". UASLP
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Bertha Torres-Alvarez, M.D.
Organizational Affiliation
Hospital Central "Dr. Ignacio Morones Prieto". UASLP
Official's Role
Study Chair
Facility Information:
Facility Name
Dermatology Department. Hospital Central "Dr. Ignacio Morones Prieto"
City
San Luis Potosí
ZIP/Postal Code
78210
Country
Mexico
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Juan Pablo Castanedo-Cazares, M.D.
Phone
52014448342795
Email
castanju@yahoo.com
First Name & Middle Initial & Last Name & Degree
Bertha Torres-Alvarez, M.D.
Phone
52014448342795
Email
torresmab@yahoo.com.mx

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
PubMed Identifier
19438997
Citation
Moncada B, Sahagun-Sanchez LK, Torres-Alvarez B, Castanedo-Cazares JP, Martinez-Ramirez JD, Gonzalez FJ. Molecular structure and concentration of melanin in the stratum corneum of patients with melasma. Photodermatol Photoimmunol Photomed. 2009 Jun;25(3):159-60. doi: 10.1111/j.1600-0781.2009.00425.x.
Results Reference
background
PubMed Identifier
18419607
Citation
Hernandez-Barrera R, Torres-Alvarez B, Castanedo-Cazares JP, Oros-Ovalle C, Moncada B. Solar elastosis and presence of mast cells as key features in the pathogenesis of melasma. Clin Exp Dermatol. 2008 May;33(3):305-8. doi: 10.1111/j.1365-2230.2008.02724.x.
Results Reference
background
PubMed Identifier
15304189
Citation
Espinal-Perez LE, Moncada B, Castanedo-Cazares JP. A double-blind randomized trial of 5% ascorbic acid vs. 4% hydroquinone in melasma. Int J Dermatol. 2004 Aug;43(8):604-7. doi: 10.1111/j.1365-4632.2004.02134.x.
Results Reference
background

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Clinical Trial of Hydroquinone Versus Miconazol in Melasma

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