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Evaluation of Tolerability, Efficacy and Adherence to Treatment With Wynzora Cream

Evaluation of Tolerability, Efficacy and Adherence to Treatment With Wynzora Cream in Patients With Psoriasis Previously Treated With Enstilar Foam.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06180473
Acronym
psowyn
Enrollment
30
Registered
2023-12-22
Start date
2024-01-01
Completion date
2024-06-30
Last updated
2025-09-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Psoriasis

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.

Interventions

OTHERquestionnaire

PPQ, TTAQ PTCS

Sponsors

Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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;

Exclusion criteria

* 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.

Design outcomes

Primary

MeasureTime frameDescription
preference of wynzora cream1 monthPercentage 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.

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026