CTRI/2023/07/055462RecruitingNot Applicable
An Immuno-Dermatological disease registry to understand the burden of Atopic dermatitis (AD), Alopecia areata (AA), and Vitiligo in Indian Patients
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Pfizer Ltd
- Enrollment
- 3,000
- Locations
- 4
- Primary Endpoint
- to evaluate the epidemiological burden of mild, moderate and severe AD,vitiligo,and AA across enrolled dermatology centers
Study Overview
Brief Summary
The objective of this registry is to evaluate the epidemiological burden of mild, moderate and severe AD, vitiligo, and AA across enrolled dermatology centers.
Elucidate the current diagnostic criteria and grading modalities for AD, vitiligo, and AA in India.
There is no study-related intervention.
Study Design
- Study Type
- Observational
Eligibility Criteria
- Ages
- 2.00 Year(s) to 64.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Be aged between 2 and 64 years old.
- •Clinical diagnosis of Vitiligo, AA or AD.
- •Evidence of a personally signed and dated informed consent/assent document indicating that the patient (or a legally acceptable representative) has been informed of all pertinent aspects of the study.
Exclusion Criteria
- •Patients meeting any of the following criteria will not be included in the study:
- •Not willing to provide written informed consent.
- •Not willing for a follow-up visit.
Outcomes
Primary Outcomes
to evaluate the epidemiological burden of mild, moderate and severe AD,vitiligo,and AA across enrolled dermatology centers
Time Frame: followup visits take place at intervals at the investigators discretion.
Secondary Outcomes
- To elucidate the current diagnostic criteria and grading modalities for AD,vitiligo,and AA in India.(followup visits take place at intervals at the investigators discretion.)
Investigators
Study Sites (4)
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