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| Tracking Information | |||||
|---|---|---|---|---|---|
| First Received Date ICMJE | July 11, 2007 | ||||
| Last Updated Date | March 5, 2009 | ||||
| Start Date ICMJE | November 2006 | ||||
| Primary Completion Date | October 2008 (final data collection date for primary outcome measure) | ||||
| Current Primary Outcome Measures ICMJE |
Time to relapse during the Maintenance Phase | ||||
| Original Primary Outcome Measures ICMJE | Same as current | ||||
| Change History | Complete list of historical versions of study NCT00500162 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE |
Subject's Quality of Life questionnaire (MelasQol)at the end of each treatment phase/Early termination. | ||||
| Original Secondary Outcome Measures ICMJE |
Subject’s Quality of Life questionnaire (MelasQol)at the end of each treatment phase/Early termination. | ||||
| Descriptive Information | |||||
| Brief Title ICMJE | Comparison of Two Tri-Luma® Maintenance Regimens in the Treatment of Melasma | ||||
| Official Title ICMJE | Comparison of Two Tri-Luma® Maintenance Regimens in the Treatment of Melasma | ||||
| 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®. |
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| 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) |
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| Study Phase | Phase IV | ||||
| Study Type ICMJE | Interventional | ||||
| Study Design ICMJE | Treatment, Randomized, Single Blind (Investigator), Active Control, Parallel Assignment, Safety/Efficacy Study | ||||
| Condition ICMJE | Melasma | ||||
| Intervention ICMJE | Behavioral: Tri-Luma Maintenance regimen | ||||
| Study Arms / Comparison Groups | |||||
| Publications * | |||||
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* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Completed | ||||
| Enrollment ICMJE | 340 | ||||
| Completion Date | October 2008 | ||||
| Primary Completion Date | October 2008 (final data collection date for primary outcome measure) | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||
| Ages | 18 Years and older | ||||
| Accepts Healthy Volunteers | No | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | Brazil, Mexico | ||||
| Administrative Information | |||||
| NCT ID ICMJE | NCT00500162 | ||||
| Responsible Party | Gladerma, Galderma | ||||
| Study ID Numbers ICMJE | RD.03.SPR.29059 | ||||
| Study Sponsor ICMJE | Galderma | ||||
| Collaborators ICMJE | |||||
| Investigators ICMJE |
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| Information Provided By | Galderma | ||||
| Verification Date | March 2009 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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