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NOT YET RECRUITING
NCT07432386
PHASE4

Methotrexate Versus Apremilast for Pruritus in Psoriasis

Sponsor: Zarmeen Khawar

View on ClinicalTrials.gov

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.

Official title: Comparison of Efficacy of Methotrexate Versus Apremilast in the Treatment of Pruritus in Psoriasis: A Randomized Controlled Trial

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

80

Start Date

2026-02-20

Completion Date

2026-07-20

Last Updated

2026-02-25

Healthy Volunteers

No

Interventions

DRUG

Apremilast

Oral Apremilast titrated to 30 mg twice daily for 8 weeks.

DRUG

Methotrexate

Oral Methotrexate 10 mg once weekly for 8 weeks.

Locations (1)

Pak Emirates Military Hospital

Rawalpindi, Punjab Province, Pakistan