Dermatology out patient clinic, Faculty of Medicine, Cairo University, Cairo, 11562, Egypt - 15 Mar `26The Value of Adding Mini-oral Pulse Steroid Therapy in Preventing Peri-lesional Halo Post Non-cultured Epidermal Cell Suspension (NCES) in Cases With Stable Segmental and Non-acral Vitiligo.

The Value of Adding Mini-oral Pulse Steroid Therapy in Preventing Peri-lesional Halo Post Non-cultured Epidermal Cell Suspension (NCES) in Cases With Stable Segmental and Non-acral Vitiligo.

Official title: The Value of Adding Mini-oral Pulse Steroid Therapy in Preventing Peri-lesional Halo Post Non-cultured Epidermal Cell Suspension (NCES) in Cases With Stable Segmental and Non-acral Vitiligo: An Interventional Prospective Randomized Controlled Trial.

Status: Opening soon

Description:

The goal of this clinical trial is to learn if adding mini-oral pulse steroid therapy improves the results of non-cultured epidermal cell suspension (NCES) surgery in patients with stable vitiligo. It will also evaluate the safety of this treatment approach. The main questions it aims to answer are: • Does adding mini-oral pulse steroid therapy reduce the development of a perilesional halo after NCES surgery? • Does the addition of steroids improve the degree of repigmentation and overall treatment outcomes in vitiligo lesions? Researchers will compare NCES surgery with mini-oral pulse steroids to NCES surgery alone to determine whether the steroid therapy improves surgical outcomes. Participants will: • Undergo NCES vitiligo surgery for stable segmental or non-acral vitiligo lesions. • Be randomly assigned to receive either surgery alone or surgery plus low-dose oral mini-pulse dexamethasone therapy. • Attend follow-up visits and clinical assessments for approximately 4 months. • Receive excimer laser sessions twice weekly after healing and have standardized photographs and scoring assessments to evaluate repigmentation.

Phase: Phase 4.

What is being studied: procedure — Non-cultured epidermal cell suspension (NCES) surgery; drug — Oral mini pulse; device — Excimer Sessions.

Who can take part: ages 12 Years, 60 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 15 March 2026 and was due to finish 01 July 2026.

Source: ClinicalTrials.gov, NCT07472816 (https://clinicaltrials.gov/study/NCT07472816).

Start date: March 15, 2026

Completion date: July 01, 2026

Organizer: Cairo University

Link: https://clinicaltrials.gov/study/NCT07472816

The registry does not list a contact for this study. Use the link above to reach the study record on ClinicalTrials.gov.

Clinical Trial Alerts

Sign up and be the first to know about updates on this trial.

This request will be sent with the trial reference The Value of Adding Mini-oral Pulse Steroid Therapy in Preventing Peri-lesional Halo Post Non-cultured Epidermal Cell Suspension (NCES) in Cases With Stable Segmental and Non-acral Vitiligo. . By submitting you agree to our Privacy Policy.

FAQOther Questions

  • Any link between vitiligo and military service?

    While there isn't specific research directly linking military service to the onset of vitiligo, it's critical to comprehend that vitiligo is a multifaceted disorder influenced b...

  • Diabetes and Vitiligo: Is There a Connection?

    Yes, there appears to be a real connection between vitiligo and diabetes, especially type 1 diabetes. A recent study using UK Biobank data also found an association with type 2 ...

  • Is vitiligo contagious?

    Vitiligo is not contagious. This means it cannot be spread from person to person through physical contact, sharing personal items, or any other means of transmission. Vitiligo i...