Comparison of Two Tri-Luma® Maintenance Regimens in the Treatment of Melasma (CLARA)
Primary Purpose
Melasma
Status
Completed
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
Tri-Luma Maintenance regimen
Sponsored by
About this trial
This is an interventional treatment trial for Melasma
Eligibility Criteria
Inclusion Criteria:
- Subjects with a clinical diagnosis of moderate to severe Melasma
- Subjects with a Fitzpatrick skin type between I and V
Exclusion Criteria:
- Female subjects who are pregnant or planning a pregnancy during the study;
- Subjects with a wash-out period for topical treatments on the treated areas less than 2 weeks for corticosteroids, glycolic Acid (in daily care cream, Bleaching products, UV light therapy and sunbathing, Topical retinoids including retinol, and less than 3 months for Lasers, IPL, dermabrasion, peeling
- Subjects with a wash-out period for systemic treatments less than 1 month for Corticosteroids and hormone-replacement therapies (unless subjects have been on treatment for at least 3 months)
- Subjects who foresee intensive UV exposure during the study (mountain sports, UV radiation, sunbathing, etc...);
Sites / Locations
- UNIFESP - Universidade Federal de São Paulo
- Hospital General de México - Servicio de Dermatología
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
1
2
Arm Description
Outcomes
Primary Outcome Measures
Time to relapse during the Maintenance Phase
Secondary Outcome Measures
Subject's Quality of Life questionnaire (MelasQol)at the end of each treatment phase/Early termination.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00500162
Brief Title
Comparison of Two Tri-Luma® Maintenance Regimens in the Treatment of Melasma
Acronym
CLARA
Official Title
Comparison of Two Tri-Luma® Maintenance Regimens in the Treatment of Melasma
Study Type
Interventional
2. Study Status
Record Verification Date
March 2009
Overall Recruitment Status
Completed
Study Start Date
November 2006 (undefined)
Primary Completion Date
October 2008 (Actual)
Study Completion Date
October 2008 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Galderma R&D
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Melasma is an acquired, symmetric, irregular hypermelanosis on sun-exposed areas of the face, commonly seen in Latin American women. It is a very frequent disease, although its true incidence is unknown.
Melasma has historically been difficult to treat and therapy remains a challenge for this chronic condition.
Melasma being a relapsing disease, there is a real need to address how to maintain efficacy achieved after acute treatment. A previous 12-month trial has shown that Tri-Luma® applied once daily over a long-term period is safe and tolerable. However, there are no robust data available either on the efficacy of Tri-Luma® in long-term treatment or guidance for a maintenance dosage regimen with this product.
Investigations have been made through a feasibility work among Dermatologists from USA and Latin America to assess their current practice in terms of Maintenance Therapy. Two regimens appear to be prescribed frequently and will be compared in this study.
The expectation is that Tri-Luma® will be effective, in one of the two regimens explored, in maintaining the Melasma improvement achieved with a previous treatment of Tri-Luma®.
Detailed Description
This study will last 32 weeks (8 months) as a maximum. 11 visits will take place (Last visit of Initial Treatment Phase = Baseline of Maintenance Phase) Initial Treatment Phase : Visit 1 (Baseline), 2 (Week 2), 3 (Week 4), 4 (Week 6), 5 (Week 8), Maintenance Phase : Visit 1 (Baseline), 2 (Week 4), 3 (Week 8), 4 (Week 12), 5 (Week 16), 6 (Week 20) , 7 (Week 24)
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Melasma
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
340 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Title
2
Arm Type
Active Comparator
Intervention Type
Behavioral
Intervention Name(s)
Tri-Luma Maintenance regimen
Primary Outcome Measure Information:
Title
Time to relapse during the Maintenance Phase
Secondary Outcome Measure Information:
Title
Subject's Quality of Life questionnaire (MelasQol)at the end of each treatment phase/Early termination.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Subjects with a clinical diagnosis of moderate to severe Melasma
Subjects with a Fitzpatrick skin type between I and V
Exclusion Criteria:
Female subjects who are pregnant or planning a pregnancy during the study;
Subjects with a wash-out period for topical treatments on the treated areas less than 2 weeks for corticosteroids, glycolic Acid (in daily care cream, Bleaching products, UV light therapy and sunbathing, Topical retinoids including retinol, and less than 3 months for Lasers, IPL, dermabrasion, peeling
Subjects with a wash-out period for systemic treatments less than 1 month for Corticosteroids and hormone-replacement therapies (unless subjects have been on treatment for at least 3 months)
Subjects who foresee intensive UV exposure during the study (mountain sports, UV radiation, sunbathing, etc...);
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Karime HASSUN, MD
Organizational Affiliation
UNIFESP - Universidade Federal de São Paulo
Official's Role
Principal Investigator
Facility Information:
Facility Name
UNIFESP - Universidade Federal de São Paulo
City
Sao Paulo
Country
Brazil
Facility Name
Hospital General de México - Servicio de Dermatología
City
Mexico City
Country
Mexico
12. IPD Sharing Statement
Learn more about this trial
Comparison of Two Tri-Luma® Maintenance Regimens in the Treatment of Melasma
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