Long-term Follow-up in Patients Affected With Acrofacial Vitiligo
NCT ID: NCT01459055
Last Updated: 2016-05-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
100 participants
OBSERVATIONAL
2016-05-31
2020-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
2. Presence of acrofacial vitiligo;
3. Able to comprehend and willing to provide written informed consent in accordance with institutional and regulatory guidelines.
Exclusion Criteria
2 -Inability to complete survey
18 Years
ALL
No
Sponsors
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Irmandade da Santa Casa de Misericordia de Curitiba
OTHER
Responsible Party
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Caio Cesar Silva de Castro
MD, PhD
Principal Investigators
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Caio C Silva de Castro, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Irmandade da Santa Casa de Misericórdia de Curitiba
Locations
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Irmandade da Santa Casa de Misericórdia de Curitiba
Curitiba, Paraná, Brazil
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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ACRO01
Identifier Type: -
Identifier Source: org_study_id
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