ClinicalTrials.Veeva

Menu

IL35 Level in Vitiligo

Cairo University (CU) logo

Cairo University (CU)

Status

Not yet enrolling

Conditions

IL35, Vitiligo

Treatments

Diagnostic Test: IL 35 in tissue biopsy

Study type

Observational

Funder types

Other

Identifiers

NCT05980390
IL35 in vitiligo

Details and patient eligibility

About

The aim of this observational study is to evaluate the level of the IL-35 protein in tissue biopsy from patients with active & stable vitiligo.

Enrollment

84 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with active and stable vitiligo

Exclusion criteria

  • Pregnant and lactating women.
  • Patients with associated autoimmune or other dermatological diseases e.g., Alopecia areata and lupus erythematous.
  • Patients already on both topical and systemic treatment at the time of recruitment.
  • Patients on Immunosuppressive drugs.
  • Other hypopigmented diseases such as pityriasis alba, tinea versicolor, lichen sclerosis, post inflammatory hypopigmentation and leprosy as excluded by lack of accentuation by wood's light examination.

Trial design

84 participants in 3 patient groups

Active vitiligo
Treatment:
Diagnostic Test: IL 35 in tissue biopsy
Stable vitiligo
Treatment:
Diagnostic Test: IL 35 in tissue biopsy
Normal controls
Treatment:
Diagnostic Test: IL 35 in tissue biopsy

Trial contacts and locations

0

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems