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Completed

NCT Number: NCT07775105

Comparative Study of Topical Pentoxifylline Versus Topical 5-Fluorouracil Combined With Microneedling and NB-UVB for Stable Vitiligo

This randomized, single-blinded clinical trial evaluates the efficacy and safety of topical pentoxifylline compared with topical 5-fluorouracil, both combined with microneedling and narrow-band ultraviolet B (NB-UVB) phototherapy, in patients with stable vitiligo. A total of 42 patients with stable vitiligo received six biweekly microneedling sessions over three months, with concomitant NB-UVB phototherapy twice weekly, followed by a three-month follow-up period. Each patient had three vitiliginous patches allocated to topical pentoxifylline with microneedling, topical 5-fluorouracil with microneedling, or microneedling alone.

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Key information

Age range

6 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Tanta University Hospitals

Tanta, Egypt

About this study

Vitiligo is a chronic depigmenting disorder characterized by depigmented macules and patches resulting from selective destruction of melanocytes. Narrow-band ultraviolet B (NB-UVB) phototherapy is an established treatment for vitiligo, while microneedling may enhance treatment response by creating microchannels that improve topical drug delivery and stimulate a wound-healing response.

This study was designed as a single-blinded comparative randomized trial involving 42 patients with stable vitiligo. Eligible patients had stable disease, defined as no new or progressive lesions for one year, and had received no treatment for at least three months. Patients with a history of keloidal or bleeding tendencies, anticoagulant therapy, pregnancy or breastfeeding, systemic or dermatological diseases, contraindications to phototherapy, photosensitive disorders, or a personal or family history of skin cancer were excluded.

In each patient, three vitiliginous patches were randomly assigned to three treatment groups. Group A received microneedling combined with topical pentoxifylline (20 mg/mL), Group B received microneedling combined with topical 5-fluorouracil (5%), and Group C received microneedling alone. Microneedling was performed every two weeks for six sessions. All groups additionally received NB-UVB phototherapy twice weekly for three months, followed by NB-UVB phototherapy alone during the subsequent three-month follow-up period.

Treatment response was assessed at baseline, at the end of treatment, and at three-month follow-up. Three blinded physicians evaluated repigmentation using the Physician Global Aesthetic Improvement Scale (GAIS). Quantitative assessment was also performed using a Visual Analog Scale (VAS) to measure percentage reduction in lesion size. Patient satisfaction and treatment-related adverse effects, including erythema, perilesional hyperpigmentation, and pain, were recorded. Participants were followed for an additional three months to assess durability of repigmentation, recurrence, and worsening of lesions.

The study found that both topical pentoxifylline and topical 5-fluorouracil, when combined with microneedling and NB-UVB, produced greater improvement than microneedling alone. Pentoxifylline showed favorable response rates, particularly for lesions on the trunk, head, and neck, and was associated with fewer adverse effects. Perilesional hyperpigmentation was more frequent with topical 5-fluorouracil.

The study was approved by the Ethics Committee under approval code 35642/8/22, and written informed consent was obtained from all participants after explanation of the study procedures, risks, and objectives.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with stable vitiligo. No new or progressive vitiligo lesions for at least 1 year. No vitiligo treatment for at least 3 months. Age 6-55 years based on the enrolled study population

Exclusion criteria

  • History of keloidal tendency. Bleeding tendency. Current anticoagulant therapy. Pregnancy or breastfeeding. Presence of other systemic or dermatological diseases. Contraindications to phototherapy. Photosensitive disorders, including lupus erythematosus or xeroderma pigmentosum.

Personal or family history of skin cancer

Treatment and study plan

Microneedling + topical treatment (PTX 20 mg/ml) followed by NB phototherapy

Combination Product

Microneedling + topical treatment (PTX 20 mg/ml) followed by NB phototherapy

Microneedling + topical treatment (5-FU 5%) followed by NB phototherapy

Combination Product

Microneedling + topical treatment (5-FU 5%) followed by NB phototherapy

Microneedling alone followed by NB phototherapy

Procedure

Microneedling alone followed by NB phototherapy

Primary outcomes

  1. Physician Global Aesthetic Improvement Scale (GAIS) score

    Time frame: After 6 treatment sessions (3 months)

    Physician-assessed percentage of repigmentation of treated vitiligo lesions using the GAIS.

Sponsors and collaborators

Lead sponsor

Tanta University

Other

Registry information

Official study title

Comparative Study of Topical Pentoxiphylline Versus Topical 5- Fluorouracil Both in Combination With Narrow- Band Ultraviolet B Phototherapy and Microneedling for the Treatment of Vitiligo

Acronym: PTX-5FU-VIT

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Aug 20, 2026
Registry last updated
Aug 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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