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Assessment of Hypoxia Inducible Factor and Autophagy Related Genes in Patients With Non-Segmental Vitiligo

S

Sohag University

Status

Enrolling

Conditions

Vitiligo

Treatments

Device: Punch Biopsy 5mm

Study type

Interventional

Funder types

Other

Identifiers

NCT06410898
Soh-Med-24-04-014MS

Details and patient eligibility

About

The present study will aim to evaluate:

  1. The presence of Hypoxia Inducible Factor in vitiligo patient
  2. Defect of Autophagy Related Genes in vitiligo patient
  3. The cross relation between Autophagy Related Genes and Hypoxia Inducible Factor in the pathogenesis of vitiligo among Egyptian patients in Sohag Governorate

Enrollment

30 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adult >18 years
  • With non segmental vitiligo
  • A group of participants will be included as a control group

Exclusion criteria

  • Pregnancy
  • Patient with chronic inflammatory skin disorders
  • patient on anti-oxidant or anti-inflammatory drugs
  • patient on topical or systemic treatment for vitiligo in last 4 weeks
  • patients with other autoimmune diseases
  • patients with diabetes mellitus

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 3 patient groups

skin biopsy from vitiligo lesion in vitiligo patient
Active Comparator group
Description:
punch biopsy 5mm from vitiligo patch in vitiligo patient
Treatment:
Device: Punch Biopsy 5mm
skin biopsy from normal skin in vitiligo patient
Active Comparator group
Description:
punch biopsy 5mm from normal skin patch in vitiligo patient
Treatment:
Device: Punch Biopsy 5mm
skin biopsy from normal skin in normal person
Active Comparator group
Description:
punch biopsy 5mm from normal skin patch in normal person
Treatment:
Device: Punch Biopsy 5mm

Trial contacts and locations

1

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Central trial contact

Rania H Metwally, Resident; Reham E El-Sharkawy, Professor

Data sourced from clinicaltrials.gov

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