drugset / Trial / NCT07432386

Methotrexate Versus Apremilast for Pruritus in Psoriasis

NCT07432386

Phase 4 Not yet recruiting 80 enrolled Zarmeen Khawar
RandomizedParallel-groupOpen-labelTreatment

Summary

This randomized controlled trial aims to compare the efficacy of Methotrexate versus Apremilast in reducing pruritus and improving quality of life in patients with psoriasis. Eighty patients aged 20 to 60 years with psoriasis involving more than 8% body surface area and associated pruritus will be enrolled and randomly assigned into two groups. Group A will receive oral Apremilast titrated to 30 mg twice daily, while Group B will receive oral Methotrexate 10 mg once weekly for 8 weeks. The primary outcome will be change in Dermatology Life Quality Index (DLQI) score at 8 weeks. Secondary outcomes include change in numerical rating scale for pruritus and assessment of adverse effects. The study will be conducted at Pakistan Emirates Military Hospital Rawalpindi.

Timeline

Start
2026-05-14
Primary completion
2026-10-14
Completion
2026-10-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Apremilast Small molecule 30 mg Oral
Subject Methotrexate Small molecule 10 mg Oral

Indications