Pre-Post Multimodal Assessment Of Severe Psoriasis Vulgaris Using Clinical, Dermoscopic And QoL Measures

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age6+
SponsorAssiut University

About this trial

The goal of this observational study is to learn about the comprehensive changes in severe plaque psoriasis (Psoriasis Vulgaris) in adult participants undergoing standard treatment. The main questions it aims to answer are: How clinical signs of psoriasis, such as redness, scaling, and thickness, change after treatment? How specific skin features, visualized under dermoscopy, change after treatment? How participants' perceptions of psoriasis-related disability and overall quality of life improve after treatment? Participants will undergo standard medical treatment for severe psoriasis. Participants will be evaluated at the beginning of the study and again after treatment using clinical skin examinations, dermoscopic imaging, and validated questionnaires (Psoriasis Disability Index and quality of life parameters).

Eligibility criteria

Qualifiers

Patients ≥ 6 years of age

Newly diagnosed patients with plaque psoriasis with affected BSA >10%

Indicated for a new systemic therapy (e.g., oral agent, biologics).

Willing and able to provide informed consent for all procedures .

Disqualifiers

• Non cooperative patients .

Pregnant or breastfeeding women

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

45 Participants
are grouped into 1 trial group

Locations

This trial has no locations

Sponsors and collaborators