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NOT YET RECRUITING
NCT07626788
NA

Pentoxifylline Add-On Therapy for Mild-to-Moderate Plaque Psoriasis

Sponsor: Wasuchon Chaichan

View on ClinicalTrials.gov

Summary

This study will evaluate whether pentoxifylline, when used as an add-on treatment to standard topical therapy, is effective and safe for adults with mild-to-moderate plaque psoriasis. Participants will be randomly assigned to receive either pentoxifylline or placebo twice daily for 12 weeks, while continuing their standard topical treatment. The study will compare improvement in psoriasis severity, itch, physician assessment, quality of life, and adverse events between the two groups. Participants will be followed for a total of 16 weeks.

Official title: Efficacy and Safety of Pentoxifylline as Add-On Therapy for Mild-to-Moderate Plaque Psoriasis: A Double-Blind Randomized Placebo-Controlled Trial

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

140

Start Date

2026-06-15

Completion Date

2028-10

Last Updated

2026-06-05

Healthy Volunteers

No

Conditions

Interventions

DRUG

Pentoxifylline 400 mg Oral Tablet

Pentoxifylline 400 mg capsule will be taken orally twice daily after meals, once in the morning and once in the evening, for 12 weeks. The intervention will be given as add-on therapy while participants continue standard topical treatment for plaque psoriasis.

DRUG

Placebo

Matching placebo capsule will be taken orally twice daily after meals, once in the morning and once in the evening, for 12 weeks. The placebo will be given as add-on therapy while participants continue standard topical treatment for plaque psoriasis.

Locations (1)

University of Phayao Hospital

Phayao, Changwat Phayao, Thailand