Azelaic Acid Iontophoresis Versus Topical Azelaic Acid Cream in the Treatment of Melasma (AAI)
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|ClinicalTrials.gov Identifier: NCT00848458|
Recruitment Status : Unknown
Verified July 2010 by Medical University of Vienna.
Recruitment status was: Recruiting
First Posted : February 20, 2009
Last Update Posted : July 15, 2010
|Condition or disease||Intervention/treatment||Phase|
|Melasma||Other: Iontophoresis Other: Azelaic acid cream||Phase 2 Phase 3|
Patients will be randomized and allocated in concealed manner to one of the two treatment arms: AAI or topical azelaic acid cream.
Azelaic acid iontophoresis treatment schedule:
Patients randomized to the AAI group will receive iontophoresis with 15% azelaic acid twice weekly over a period of 12 weeks.
Azelaic acid topical treatment schedule:
Patients randomized to the topical treatment group will receive topical treatment with 20% azelaic acid cream twice daily over a period of 12 weeks.
Besides emollients no additional specific treatments will be allowed during the study.
The use of broad spectrum (UVA+UVB) sunscreen is recommended over the entire study period (9 month).
After completion of the active study period (3 month in both treatment groups), maintenance and efficacy of both treatment schedules will be followed up quarterly over 6 month
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||70 participants|
|Intervention Model:||Parallel Assignment|
|Official Title:||Azelaic Acid Iontophoresis Versus Topical Azelaic Acid Cream in the Treatment of Melasma - An Open Randomized, Controlled, Prospective, Single Blinded Clinical Trial|
|Study Start Date :||January 2009|
|Estimated Primary Completion Date :||December 2010|
|Experimental: Azelaic Acid Iontophoresis||
iontophoresis with 15% azelaic acid gel twice weekly
|Active Comparator: Azelaic acid topical||
Other: Azelaic acid cream
topical treatment with 20% azelaic acid cream twice daily
- Change in colorimetric measurement of skin colour and MASI-Score after 12 weeks of treatment [ Time Frame: 3 month ]
- Physician Global Assessment, Patient Global Assessment, Overall Response Assessment [ Time Frame: 3 month ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00848458
|Contact: Oliver Schanab, MD||004340400 ext firstname.lastname@example.org|
|Medical University Vienna / Depatment of Dermatology||Recruiting|
|Vienna, Austria, 1180|
|Contact: Oliver Schanab, MD 004340400 ext 5441 email@example.com|
|Principal Investigator: JB Schmidt, MD|
|Sub-Investigator: Oliver Schanab, MD|
|Sub-Investigator: Anna Pinkowicz, MD|
|Principal Investigator:||JB Schmidt, MD||MUV|
|Study Director:||Oliver Schanab, MD||MUV|