IL35 Level in Vitiligo

NCT ID: NCT05980390

Last Updated: 2023-08-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

84 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-08-10

Study Completion Date

2023-10-30

Brief Summary

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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.

Detailed Description

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Conditions

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IL35, Vitiligo

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Active vitiligo

IL 35 in tissue biopsy

Intervention Type DIAGNOSTIC_TEST

Elisa testing

Stable vitiligo

IL 35 in tissue biopsy

Intervention Type DIAGNOSTIC_TEST

Elisa testing

Normal controls

IL 35 in tissue biopsy

Intervention Type DIAGNOSTIC_TEST

Elisa testing

Interventions

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IL 35 in tissue biopsy

Elisa testing

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Cairo University

OTHER

Sponsor Role lead

Responsible Party

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Hagar El Sayed

Dr

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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IL35 in vitiligo

Identifier Type: -

Identifier Source: org_study_id

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