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The purpose of this study is:
To evaluate the efficacy of the drugs under study for treating chronic plaque psoriasis.
- Population:
50 patients will be selected from both sexes, healthy, between 18 and 65 years with a clinical diagnosis of chronic plaque psoriasis with PASI <20%, according to the criteria of inclusion and exclusion.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Tazarotene 0.1% |
| ||
| Calcipotriol 0.005% |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Each patient will receive a sample of the drug test (tazarotene 0.1%) and a control sample of the drug (calcipotriene 0.005%). | Drug | Apply the medication once daily, preferably at night, in quantities sufficient to cover only the lesions with a thin layer of the product (an average of 2 mg/cm2).Apply only in lesions of the right hemisphere. |
Inclusion Criteria:
Exclusion Criteria:
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50 patients will be selected from both sexes, healthy, between 18 and 65 years with a clinical diagnosis of chronic plaque psoriasis with PASI <20%, according to the criteria of inclusion and exclusion.
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| Name | Affiliation | Role |
|---|---|---|
| Sergio Schalka | Medcin Instituto da Pele Ltda | Principal Investigator |
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| ID | Term |
|---|---|
| C086827 | tazarotene |
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