Gene Polymorphism in Tinea Versicolor

April 22, 2021 updated by: Rana F Hilal, MD, Kasr El Aini Hospital

Detection of IL1-7A and IL-17F Gene Polymorphism in Pityriasis Versicolor and Its Relation to Susceptibility to Infections.

Blood samples will be taken from cases presenting with recurrent tinea versicolor , after confirmation of diagnosis by wood's light and KOH examination, for the detection of gene polymorphism in IL17 A and IL17 F.

In addition , serum samples from patients and controls will be tested for 25(OH)2 D3

Study Overview

Status

Recruiting

Study Type

Observational

Enrollment (Anticipated)

200

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • El Manial
      • Cairo, El Manial, Egypt, 11956
        • Recruiting
        • Kasr Al Ainy Hospital, Cairo university
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 60 years (Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients with history of disseminated TV, with 2 or more episodes of TV per year.

Description

Inclusion Criteria:

  • - Patients with recurrent pityriasis versicolor (active now) and not taking treatment for it.
  • Patients of both genders.
  • Age ≥18 years old.

Exclusion Criteria:

  • - Patients with other cutaneous diseases.
  • Patient's having dandruff (scaly scalp) even if not symptomatizing.
  • Pregnant and lactating females, children, prisoners, cognitively impaired or mentally disabled subjects.
  • Patients with autoimmune diseases.
  • Patients with immunodeficiency diseases.
  • Immunosuppressed patients e.g. HIV, diabetics, organ transplant, malignancy, patients taking immunosuppressive drugs e.g. chemotherapy, cortisone.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Control
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Patients with recurrent pityriasis versicolor
Healthy age and sex-matched controls

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
IL 17A gene polymorphism
Time Frame: 6months-1 year
IL 17A
6months-1 year
IL 17 F gene polymorphism
Time Frame: 6months-1 year
IL 17 F
6months-1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Vitamin D
Time Frame: 6months-1 year
Serum 25(OH)2 D3
6months-1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 1, 2019

Primary Completion (Anticipated)

June 1, 2021

Study Completion (Anticipated)

November 1, 2021

Study Registration Dates

First Submitted

February 21, 2021

First Submitted That Met QC Criteria

February 21, 2021

First Posted (Actual)

February 25, 2021

Study Record Updates

Last Update Posted (Actual)

April 26, 2021

Last Update Submitted That Met QC Criteria

April 22, 2021

Last Verified

February 1, 2021

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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