Thymic Stromal Lymphopoietin (TSLP) in Vitiligo
Study of the Cutaneous Expression of Thymic Stromal Lymphopoietin (TSLP) in a Sample of Vitiligo Patients
1 other identifier
interventional
50
0 countries
N/A
Brief Summary
study \& verify the hypothesis of the involvement of TSLP in the pathogenesis of vitiligo in comparison to their levels in the healthy control persons.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2017
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2017
CompletedFirst Submitted
Initial submission to the registry
December 5, 2017
CompletedFirst Posted
Study publicly available on registry
December 8, 2017
CompletedDecember 20, 2017
December 1, 2017
6 months
December 5, 2017
December 18, 2017
Conditions
Outcome Measures
Primary Outcomes (1)
Expression levels of TSLP in patients of Vitiligo.
7 months
Study Arms (2)
vitiligo patients
EXPERIMENTALcontrols
EXPERIMENTALInterventions
Lesional skin biopsy was taken from every patient. Also a skin biopsy was taken from every control subject
Eligibility Criteria
You may qualify if:
- Patients with generalized non-segmental vitiligo.
- Both sexes.
- Age \< 18 years old age.
- New cases or cases not receiving any medication for at least 3 months ago.
You may not qualify if:
- Age: Patients \< 18 years.
- Segmental or universal vitiligo.
- Pregnant and lactating females. Autoimmune diseases
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr
Study Record Dates
First Submitted
December 5, 2017
First Posted
December 8, 2017
Study Start
January 1, 2017
Primary Completion
July 1, 2017
Study Completion
July 1, 2017
Last Updated
December 20, 2017
Record last verified: 2017-12