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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03371758
Other study ID # Dermatology
Secondary ID
Status Recruiting
Phase N/A
First received December 5, 2017
Last updated January 19, 2018
Start date January 2017
Est. completion date May 2018

Study information

Verified date January 2018
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The exact mechanism of impairment of autophagy in vitiligo has not yet been determined.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date May 2018
Est. primary completion date May 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 12 Years and older
Eligibility Inclusion Criteria:

- • Patients with non-segmental vitiligo whether active or stable.

- Age above 12 years.

- Both sexes.

Exclusion Criteria:

- • Patients should not use any topical or systemic treatment at least 6 weeks before inclusion into the study.

- Patients having other autoimmune disease, heart disease, liver disease, kidney disease, neurological disorder, cancer, active infection or any chronic disease.

- Pregnancy or breast feeding for female patients.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
skin biopsy
Punch skin biopsy will be taken from the lesional and non-lesional skin of vitiligo patients as well as healthy skin of controls.

Locations

Country Name City State
Egypt Maha Fathy Elmasry Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Expression of LC3-I, LC3-II & Beclin 1 in vitiligo patients 1 year
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