Long-term Follow-up in Patients Affected With Acrofacial Vitiligo

NCT ID: NCT01459055

Last Updated: 2016-05-03

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-05-31

Study Completion Date

2020-08-31

Brief Summary

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Acrofacial vitiligo is a clinical form of vitiligo characterized by macules in distal digits, periorificial-facial and ano-genital areas. Vitiligo European Task Force classifies vitiligo as generalized or localized; generalized vitiligo may be further sub-divided into acrofacial, vulgaris and universalis, and localized vitiligo, into segmental and focal. Some authors do not believe that acrofacial is a real vitiligo clinical form, considering it as an initial form of vulgaris vitiligo. The aim of this study is to follow early- diagnosed acrofacial patients during ten years in order to define if these patients will maintain this clinical form or will evolute to a more severe clinical form.

Detailed Description

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Conditions

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Vitiligo

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

1. Patients of both genders, aged older than years, able to understand and provide written informed consent and able to allow compliance at the treatment and the requirements of the protocol;
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

1- Subjects assessed as not suitable for the study in the opinion of the investigator

2 -Inability to complete survey
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Irmandade da Santa Casa de Misericordia de Curitiba

OTHER

Sponsor Role lead

Responsible Party

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Caio Cesar Silva de Castro

MD, PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

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

Site Status

Countries

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Brazil

Central Contacts

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Caio Cesar C Castro, MD, PhD

Role: CONTACT

00554135682036

Facility Contacts

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Caio Cesar Silva de Castro, MD, PhD

Role: primary

00554135682036

Other Identifiers

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ACRO01

Identifier Type: -

Identifier Source: org_study_id

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