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Evaluation of Serum Interleukin-15 and Interleukin-22 Levels in Patients With Non-segmental Vitiligo

Evaluation of Serum Interleukin-15 and Interleukin-22 Levels in Patients With Non-segmental Vitiligo

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05121532
Enrollment
60
Registered
2021-11-16
Start date
2022-01-31
Completion date
2022-12-31
Last updated
2021-11-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vitiligo

Brief summary

Evaluation of Serum Interleukin-15 and Interleukin-22 Levels in Patients with Non-segmental Vitiligo before and after phototherapy

Detailed description

This prospective study will include 30 patients with NSV, attending the Outpatient Clinics of Dermatology at Sohag University Hospitals, as well as 30 normal volunteers as control. This study will be submitted for approval by Research and Ethical committees at Sohag Faculty of Medicine. An informed written consent will be obtained from each subject prior to participation in the study after full explanation of the procedure.

Interventions

DIAGNOSTIC_TESTInterleukin-15 and Interleukin-22

Serum Interleukin-15 and Interleukin-22 in non segmental vitiligo

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* • Patients suffering from non segmental vitiligo. * Patients not on medical treatment or phototherapy for vitiligo in the last 3 months.

Exclusion criteria

* • Patients with systemic or cutaneous inflammatory disorders. * Patients on treatment for vitiligo in last 3 months. * Pregnant and lactating patients. * Patients with history of diabetes. * Patients with history of autoimmune diseases.

Design outcomes

Primary

MeasureTime frameDescription
Evaluation of Serum Interleukin-15 and Interleukin-22 Levels3 months3 ml venous blood will be obtained from participante using commerciall available double antibody sandwich enzyme-linked immunosorbent assay (ELISA) kits to evaluate 1. Serum IL15 level . 2. Serum IL22 level. 3 ml venous blood will be obtained from participante using commerciall available double antibody sandwich enzyme-linked immunosorbent assay (ELISA) kits to evaluate 1\. Serum IL15 level . 2. Serum IL22 level.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026