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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05335746
Other study ID # Rc 6-2022
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 10, 2022
Est. completion date September 30, 2022

Study information

Verified date April 2022
Source Benha University
Contact Ahmed Abdelshafy, MD
Phone 01222328766
Email ahmad4lg@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Vitiligo patients on systemic and local therapy may have some ocular adverse effects associated with the disease and its therapy.


Description:

Chorioretinal changes associated with vitiligo therapy could address patients visual acuity and life style. Early detection of these changes can help these patients to evade such adverse effects.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date September 30, 2022
Est. primary completion date September 30, 2022
Accepts healthy volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - vitiligo patients on systemic and local therapy that regularly visit dermatology clinic at banha university. - normal subjects seeking regular ophthalmic examination at ophthalmology clinic at banha university. Exclusion Criteria: - patients with known chronic retinal diseases that may alter OCT-A parameters as age related macular degeneration and diabetic retinopathies. - patients that refuse to participate in this study.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Optical coherence tomography angiography (OCT-A)
Optical coherence tomography angiography scanning will be done for all subjects in the study.

Locations

Country Name City State
Egypt Benha University Banha QA

Sponsors (1)

Lead Sponsor Collaborator
Benha University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Other Changes in visual acuity Visual acuity measurements in decimal form Immediately after OCT-A for each eye and at one month of follow-up.
Other Changes in choroidal thickness Choroidal thickness in mm. Immediately after OCT-A for each eye and at one month of follow-up.
Primary Percentage of vessel density (VD) in superficial and deep retinal layer. Percentage (%) of superficial and deep vessel density changes in both groups measured by OCT-A software to asses retinal ischemia. Immediately after OCT-A for each eye and at one month of follow-up.
Secondary Foveal avascular zone (FAZ) in millimeter (mm). Foveal avascular zone measurement in both groups in mm measured by OCT-A software. Immediately after OCT-A for each eye and at one month of follow-up.
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