Evaluation of Tolerability, Efficacy and Adherence to Treatment With Wynzora Cream
- Conditions
- Psoriasis
- Registration Number
- NCT06180473
- Brief Summary
The primary objective is to assess with the PPQ questionnaire the patient preference for Wynzora compared with therapy carried out previously with Enstilar spray foam. Secondary objectives Assess satisfaction with the treatment. Assess adherence to therapy. Evaluate the impact of various clinical and demographic factors on treatment adherence. Evaluate the efficacy of Wynzora cream therapy.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 30
- Patients older than 18 years of age, of either sex;
- Patients diagnosed with mild-to-moderate psoriasis (PASI and BSA <10) requiring monotherapy topical with Wynzora;
- Patients who have stopped treatment with Enstilar foam for any reason for at least 30 days; and
- Patients whose medical records are accessible and record all demographic parameters, anthropometric and clinical parameters during the treatment period
- Signature of written informed consent;
- Patients with palmoplantar, inverse, erythrodermic, guttate, and scalp psoriasis.
- Patients who are taking concomitant systemic therapies for psoriasis, such as. cyclosporine, methotrexate, acitretin, phototherapy or biologic therapies.
- Women who are pregnant or planning to become pregnant.
- Patients with disabilities or other motor problems that could complicate self-medication.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method preference of wynzora cream 1 month Percentage of patients who prefer treatment with Wynzora compared with treatment with Enstilar at week 4 of use; preference for Wynzora will be assessed by considering a score of 3 or higher on question 5 of the PPQ questionnaire.
- Secondary Outcome Measures
Name Time Method