- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01401374
Online Health Survey of Patients With Vitiligo Vulgaris/ Online Survey of Pediatric Patients With Vitiligo
April 7, 2017 updated by: St. Luke's-Roosevelt Hospital Center
The study is an on-line survey posted on survey monkey that addresses some demographic and environmental issues that could potentially relate to vitiligo vulgaris onset or disease exacerbation.
Study Overview
Status
Completed
Conditions
Detailed Description
The survey is designed to look at some issues that are pertinent to individuals with vitiligo, including access to care, severity of disease, under-reported disease activity, causative and exacerbating factors and co-morbid illnesses.
Study Type
Observational
Enrollment (Actual)
3258
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
-
New york, New York, United States, 10025
- St. Luke's-Roosevelt Hospital Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Individuals self-reporting vitiligo vulgaris and controls who do not have vitiligo vulgaris
Description
Inclusion Criteria:
- Ability to complete survey
Exclusion Criteria:
- Inability to complete survey
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Vitiligo Patients
patients with vitiligo vulgaris
|
|
Controls
Individuals without vitiligo vulgaris
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Correlation of Disease State in Vitiligo with Clinical and Psychological Measures
Time Frame: Self-reported retrospective single survey
|
Self-reported retrospective single survey
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Nanette Silverberg, MD, St. Luke's-Roosevelt Hospital Center
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Silverberg JI, Reja M, Silverberg NB. Regional variation of and association of US birthplace with vitiligo extent. JAMA Dermatol. 2014 Dec;150(12):1298-305. doi: 10.1001/jamadermatol.2014.899.
- Silverberg JI, Silverberg NB. Quality of life impairment in children and adolescents with vitiligo. Pediatr Dermatol. 2014 May-Jun;31(3):309-18. doi: 10.1111/pde.12226. Epub 2013 Oct 18.
- Silverberg JI, Silverberg NB. Association between vitiligo extent and distribution and quality-of-life impairment. JAMA Dermatol. 2013 Feb;149(2):159-64. doi: 10.1001/jamadermatol.2013.927.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2011
Primary Completion (Actual)
March 1, 2016
Study Completion (Actual)
March 1, 2016
Study Registration Dates
First Submitted
July 21, 2011
First Submitted That Met QC Criteria
July 22, 2011
First Posted (Estimate)
July 25, 2011
Study Record Updates
Last Update Posted (Actual)
April 10, 2017
Last Update Submitted That Met QC Criteria
April 7, 2017
Last Verified
April 1, 2017
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 10-148/10-149x
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Vitiligo Vulgaris
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-
Centre Hospitalier Universitaire de NiceNot yet recruiting
-
University of TorontoCanadian Interdisciplinary Network Complementary & Alternative Medicine ResearchCompleted
-
University Hospital, GhentNovartisCompletedVitiligo VulgarisBelgium
-
Assiut UniversityUnknown
-
St. Luke's-Roosevelt Hospital CenterBeth Israel Medical CenterCompleted
-
Szeged UniversityRecruitingPsoriasis | Atopic Dermatitis | Alopecia Areata | Vitiligo VulgarisHungary
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PfizerActive, not recruitingStable Nonsegmental Vitiligo | Active Nonsegmental VitiligoUnited States, Spain, China, Puerto Rico, Australia, Canada, Hungary, United Kingdom, Taiwan, Japan, Slovakia, Bulgaria, Germany, Belgium, Mexico, Italy, Poland, Turkey (Türkiye)
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Hudson BiotechRecruitingNonSegmental Vitiligo | Nonsegmental Vitiligo (Stable)China