Xijing Hospital, Xi'an, Shaanxi, 710032, China - 01 Apr `25Oral Tacrolimus vs Dexamethasone Micro-pulse Therapy in Pediatric Rapidly Progressing Vitiligo: A Multicenter RCT

Oral Tacrolimus vs Dexamethasone Micro-pulse Therapy in Pediatric Rapidly Progressing Vitiligo: A Multicenter RCT

Official title: Oral Tacrolimus Capsule Versus Dexamethasone Micro-pulse Therapy for the Treatment of Rapidly Progressing Vitiligo in Children: A Multicenter, Randomized, Controlled Study

Status: Recruiting now

Description:

This clinical study aims to compare the safety and effectiveness of two treatments-oral Tacrolimus capsules and Dexamethasone micro-pulse therapy-in children aged 4-12 years with rapidly progressing vitiligo. The study is a multicenter, randomized, controlled trial involving 90 participants, who will be divided equally into two groups. One group will receive daily Tacrolimus, while the other will take Dexamethasone on weekends. Over 24 weeks, doctors will monitor improvements in skin repigmentation, side effects, and overall health through regular check-ups and blood tests. The goal is to determine which treatment better controls disease progression and improves quality of life for children with vitiligo. Key Points: • For children with rapidly spreading vitiligo. • Compares two common medications. • Follows participants for 6 months. • Focuses on safety and effectiveness.

What is being studied: drugs — Tacrolimus, Dexamethasone.

Who can take part: ages 4 Years to 12 Years, 90 participants planned.

Enrollment status: the registry has not updated this study since its planned completion date, so its current status is unclear. The study started 01 April 2025 and was due to finish 01 April 2026.

Contact: Zhe Jian, Associate Professor.

Source: ClinicalTrials.gov, NCT06900777 (https://clinicaltrials.gov/study/NCT06900777).

Start date: April 01, 2025

Completion date: April 01, 2026

Organizer: Xijing Hospital

Contact: Zhe Jian, Associate Professor

Tel.: +862984775406

Email: 13571826086@163.com

Link: https://clinicaltrials.gov/study/NCT06900777

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