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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05067699
Other study ID # VitD&PV
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 1, 2021
Est. completion date March 1, 2022

Study information

Verified date September 2021
Source Kasr El Aini Hospital
Contact Rana Hilal, M.D
Phone +201001488869
Email rana.hilal@kasralainy.edu.eg
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Serum Samples will be taken from patients with recurrent Pityriasis Versicolor for the evaluation of vitamin D level.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date March 1, 2022
Est. primary completion date January 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Human 25-Hydroxyvitamin D3 (HVD3) ELISA Kit (96 well)
The serum will be tested by a double-antibody sandwich enzyme-linked immunosorbent assay (ELISA) to assay the level of Human 25Dihydroxy vitamin D(25-OH-D).

Locations

Country Name City State
Egypt Kasr Al Ainy Teaching Hospital Cairo

Sponsors (1)

Lead Sponsor Collaborator
Kasr El Aini Hospital

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Serum 25(OH) D3 level The serum of patients and controls will be tested by a double-antibody sandwich enzyme-linked immunosorbent assay (ELISA) to assay the level of Human 25Dihydroxy vitamin D(25-OH-D). 6months-1 year
See also
  Status Clinical Trial Phase
Recruiting NCT04769804 - Gene Polymorphism in Tinea Versicolor