CClinicalTrials.gg
CompletedNCT07690501Updated Jul 8, 2026

Adipose-derived Stem Cells Combined With Excimer Light in the Treatment of Stable Vitiligo

An interventional study of Adipose-derived Stem Cells Combined With Excimer Light in Adipose-derived Stem Cells, Excimer Light and Stable Vitiligo, sponsored by Tanta University. Completed at 1 site in Egypt. Open to participants aged 15 Years to 52 Years. Per ClinicalTrials.gov, last updated 2026-07-08.

Sponsored by Tanta University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 2 years 11 months after the study started (first participant enrolled Aug 2023, registered Jul 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
15
Allocation
Not applicable
Ages
15 Years to 52 Years
Sex
All
01

Study summary

This study aimed to assess the efficacy and safety of intradermal injection of adipose-derived stem cells, alone and combined with excimer light in treatment of stable vitiligo.

Read the detailed description

Vitiligo is a common disfiguring autoimmune disease that negatively affects patients' self-esteem and quality of life. Vitiligo is caused by a dynamic interplay between genetic and environmental risks that initiates an autoimmune attack on melanocytes in the skin.

Adipose tissue-derived stem cells have the capacity to secrete a variable cytokines and growth factors, including hepatocyte growth factor (HGF), interleukin-6 (IL-6), macrophage colony-stimulating factor (M-CSF), transforming growth factor-β1 (TGF-β1), tumour necrosis factor (TNF), vascular endothelial growth factor (VEGF), that stimulate angiogenesis, tissue remodeling, and anti-apoptotic processes. Phototherapy has an eminent effect on stoppage of progression and repigmentaion of vitiligo patches. Narrowband ultraviolet B (NB-UVB) and ultraviolet A (UVA), and monochromatic excimer light (MEL) can be used in treatment of vitiligo. The specific 308-nm radiation wavelength is delivered in a targeted form by the xenon-chloride excimer laser and is also available in an incoherent form that is commonly referred to as the excimer lamp.

02

Conditions studied

  • Adipose-derived Stem Cells
  • Excimer Light
  • Stable Vitiligo
03

In context

Lead sponsor

Tanta University is the lead sponsor of 963 studies on the registry; 304 are open to participants now.

Of its 16 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
15 Years to 52 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patients with two or more similar patches of stable vitiligo "absence of new patches of depigmentation or enlargement of the pre-existing patches" for 6 months at least.
  • Patients who will accept to be enrolled in the study and will sign an informed consent.

Exclusion criteria

Exclusion Criteria:

  • Unstable vitiligo for more than 6 months.
  • Current bacterial or viral infection in the treatment area.
  • Patients with unrealistic expectation.
  • Very thin patients "poor donor areas".
  • Patients with uncontrolled systemic disease such as diabetes or hypertension.
  • Patients with hepatitis B or C virus infection.
  • Patients with any other skin disease.
  • Patients with bleeding or coagulopathy disorders.
  • Pregnancy and lactation.
  • Patients who received topical treatment for vitiligo during the last month, or systemic treatment during the past three months before the study.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
15 participants (actual)

Study arms

  • Experimental
    Study group

    Patients with two or more similar patches of stable vitiligo "absence of new patches of depigmentation or enlargement of the pre-existing patches" for 6 months at least

    Procedure: Adipose-derived Stem Cells Combined With Excimer Light

Interventions

  • ProcedureAdipose-derived Stem Cells Combined With Excimer Light

    All patients received adipose-derived stem cells combined with excimer light.

06

What researchers measure

Primary outcomes

  1. Vitiligo Disease Activity (VIDA) Score

    The Vitiligo Disease Activity (VIDA) Score is a 6-point clinical scale used to measure the progression or stability of vitiligo. The scale ranges from -1 to +4, where higher numbers indicate more recent and rapid disease activity: * 4: Active disease (new lesions or expansion) within the last 6 weeks. * 3: Active disease between 6 weeks and 3 months. * 2: Active disease between 3 and 6 months. * 1: Active disease between 6 and 12 months. 0: Stable disease with no changes for 1 year or longer. * 1: Stable for 1 year or longer, showing signs of spontaneous repigmentation

    Time frame: 6 months post-procedure

07

Study locations

1 site
  • Tanta University
    Tanta, El-Gharbia 31527, Egypt
08

References and documents

Individual participant data

Plan to share: Yes — The data will be available upon a reasonable request from the corresponding author after the end of study for one year.

Supporting information: Study protocol

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 8, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07690501
Lead sponsor
Tanta University
Responsible party
Samar El-Sayed Abdel Hamid Gad (Assistant Lecturer of Dermatology and Venereology, Faculty of Medicine, Tanta University, Egypt, Tanta University) — Principal investigator
First posted
Jul 8, 2026
Start date
Aug 1, 2023
Primary completion
Sep 1, 2025
Completion
Sep 1, 2025
Last update
Jul 8, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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