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Sponsored by: |
Dresden University of Technology |
---|---|
Information provided by: | Dresden University of Technology |
ClinicalTrials.gov Identifier: | NCT00236171 |
The purpose of this study is to evaluate the efficacy of the topical therapies Protopic and Advantan as well as their combination against placebo in a Psoriasis Plaque Test
Condition | Intervention |
---|---|
Psoriasis Vulgaris |
Drug: Protopic, Advantan Procedure: Blood and Urine Test Procedure: coherence tomography |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double Blind (Subject, Investigator, Outcomes Assessor), Placebo Control, Single Group Assignment, Efficacy Study |
Official Title: | Evaluation of Topical Antipsoriatics in the Psoriasis Plaque Test |
Enrollment: | 14 |
Study Start Date: | September 2004 |
Estimated Study Completion Date: | September 2008 |
Primary Completion Date: | April 2006 (Final data collection date for primary outcome measure) |
daily psoriasis plaque tests for two weeks and optical coherence tomography (OCT) and 20-MHz-ultrasound on day 0 and day 11, 10 days post end of treatment and 20 days post end of treatment
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Germany, Sachsen | |
Technische Universität Dresden | |
Dresden, Sachsen, Germany, 0351 |
Principal Investigator: | Gottfried Wozel, Professor | Technische Universität Dresden |
Responsible Party: | Technical University Dresden ( Gottfried Wozel, MD ) |
Study ID Numbers: | ETAPSO |
Study First Received: | October 4, 2005 |
Last Updated: | May 27, 2008 |
ClinicalTrials.gov Identifier: | NCT00236171 |
Health Authority: | Germany: Federal Institute for Drugs and Medical Devices |
topical therapy Psoriasis Plaque Test |
Methylprednisolone aceponate Skin Diseases Psoriasis Tacrolimus Skin Diseases, Papulosquamous |