Gasdermin D Expression in Generalized Vitiligo Patients After Narrow-band Ultraviolet B Therapy

NCT ID: NCT06546059

Last Updated: 2024-08-09

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

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-08-31

Study Completion Date

2024-11-30

Brief Summary

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The aim of this study is to:

1. Evaluate the role of tissue Gasdermin D expression using immunehistochemstry techniques in patients with generalized vitiligo and compare it with healthy controls.
2. Evaluation expression of tissue Gasdermin D using immunehistochemstry techniques in patients with generalized vitiligo after narrow band ultraviolet B therapy.
3. Determine whether there is a relationship between Gasdermin D levels and disease duration and involved body surface area (VISA) in vitiligo patients.

Detailed Description

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The aim of this study is to:

1. Evaluate the role of tissue Gasdermin D expression using immunehistochemstry techniques in patients with generalized vitiligo and compare it with healthy controls.
2. Evaluation expression of tissue Gasdermin D using immunehistochemstry techniques in patients with generalized vitiligo after narrow band ultraviolet B therapy.
3. Determine whether there is a relationship between Gasdermin D levels and disease duration and involved body surface area (VISA) in vitiligo patients.

Conditions

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Vitiligo, Generalized

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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one group

Group Type OTHER

narrow band ultraviolet-B

Intervention Type DEVICE

vitiligo patients will recevie twice sessions per week

Interventions

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narrow band ultraviolet-B

vitiligo patients will recevie twice sessions per week

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Patients with stable vitiligo of 6 months duration,
* Both sex and ages(10-75)

Exclusion Criteria

* pregnancy,
* lactation,
* patients under or previous phototherapy,
* patients on other immunosuppressives,
* patients receiving topical or systemic therapy like antioxidants and vitamins were kept off treatment for 2 weeks prior to recruitment into the study.
Minimum Eligible Age

10 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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South Valley University

OTHER

Sponsor Role lead

Responsible Party

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Soheir Abdelhamid

Soheir Abdel-Hamid, principle investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

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Soheir Abdel-Hamid, MD

Role: CONTACT

01066877343

Basma Tito Abd Elhameed, MD

Role: CONTACT

01020304210

Other Identifiers

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SVU-MED-,4-24,7,871

Identifier Type: -

Identifier Source: org_study_id

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