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Comparison of Two Tri-Luma® Maintenance Regimens in the Treatment of Melasma (CLARA)
This study has been completed.
Study NCT00500162   Information provided by Galderma
First Received: July 11, 2007   Last Updated: March 5, 2009   History of Changes

July 11, 2007
March 5, 2009
November 2006
October 2008   (final data collection date for primary outcome measure)
Time to relapse during the Maintenance Phase
Same as current
Complete list of historical versions of study NCT00500162 on ClinicalTrials.gov Archive Site
Subject's Quality of Life questionnaire (MelasQol)at the end of each treatment phase/Early termination.
Subject’s Quality of Life questionnaire (MelasQol)at the end of each treatment phase/Early termination.
 
Comparison of Two Tri-Luma® Maintenance Regimens in the Treatment of Melasma
Comparison of Two Tri-Luma® Maintenance Regimens in the Treatment of Melasma

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®.

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)

Phase IV
Interventional
Treatment, Randomized, Single Blind (Investigator), Active Control, Parallel Assignment, Safety/Efficacy Study
Melasma
Behavioral: Tri-Luma Maintenance regimen
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
340
October 2008
October 2008   (final data collection date for primary outcome measure)

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...);
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Brazil,   Mexico
 
NCT00500162
Gladerma, Galderma
RD.03.SPR.29059
Galderma
 
Principal Investigator: Karime HASSUN, MD UNIFESP - Universidade Federal de São Paulo
Galderma
March 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP