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CompletedNCT01206374Updated May 25, 2015

Questionnaire and Laboratory Data on Vitiligo Vulgaris

An observational study in Vitiligo Vulgaris, sponsored by St. Luke's-Roosevelt Hospital Center. Completed at 2 sites in United States. Per ClinicalTrials.gov, last updated 2015-05-25.

Sponsored by St. Luke's-Roosevelt Hospital Center · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
57
Sex
All
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Study summary

Vitiligo vulgaris is an autoimmune disorder that causes loss of pigmentation over the skin, hair and mucous membranes (e.g. lips, nose, genitals). While genes have been identified that are thought to be required for development of vitiligo, only 5-10% of relatives develop disease. The triggers for disease onset have not yet been identified. The intent of this study is to research trends in laboratory data, social and medical history that may be contributory to vitiligo onset, location of disease, course of illness and response to therapy.

Read the detailed description

Patients who participate in this study will be asked to complete a survey and have blood/ laboratory testing performed that relates or may relate to the diagnosis of vitiligo.

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Conditions studied

  • Vitiligo Vulgaris

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Keywords

  • Vitiligo Vulgaris
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In context

Vitiligo

298 studies on the registry are indexed under Vitiligo; 69 are open to participants now.

This study's enrollment of 57 is below the median of 111 across 60 observational studies indexed under Vitiligo.

Browse Vitiligo studies →

Lead sponsor

St. Luke's-Roosevelt Hospital Center is the lead sponsor of 68 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

All patients willing to sign consent, complete questionnaire and/ or laboratory studies.

Inclusion criteria

  • Diagnosis of Vitiligo Vulgaris
  • Ability to sign consent

Exclusion criteria

Exclusion Criteria:

  • Pregnant
  • Inability to sign consent
  • Inability to complete questionnaire
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
57 participants (actual)
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What researchers measure

Primary outcomes

  1. Quality of life disturbances in people with vitiligo

    dermatology life quality indices were you used and correlated with location of disease

    Time frame: point prevalence

Secondary outcomes

  1. self-reporting of vitiligo disease symptoms and history

    Correlation of the patient survey response with chart documentation was performed.

    Time frame: single survey

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Study locations

2 sites
  • Department of Dermatology, Beth Israel Medical Center
    New York, New York 10003, United States
  • Department of Dermatology, St. Luke's-Roosevelt Hospital Center
    New York, New York 10025, United States
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References and documents

Publications

  • Silverberg NB. Update on childhood vitiligo. Curr Opin Pediatr. 2010 Aug;22(4):445-52. doi: 10.1097/MOP.0b013e32833b6ac3. PubMed 20616733 ↗
  • Silverberg JI, Silverberg AI, Malka E, Silverberg NB. A pilot study assessing the role of 25 hydroxy vitamin D levels in patients with vitiligo vulgaris. J Am Acad Dermatol. 2010 Jun;62(6):937-41. doi: 10.1016/j.jaad.2009.11.024. PubMed 20466170 ↗
  • Pagovich OE, Silverberg JI, Freilich E, Silverberg NB. Thyroid abnormalities in pediatric patients with vitiligo in New York City. Cutis. 2008 Jun;81(6):463-6. PubMed 18666385 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 25, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01206374
Lead sponsor
St. Luke's-Roosevelt Hospital Center
Collaborators
Beth Israel Medical Center
Responsible party
Sponsor
First posted
Sep 21, 2010
Start date
Aug 2010
Primary completion
Oct 2010
Completion
Sep 2014
Last update
May 25, 2015

Study contacts

Nanette Silverberg, MD
principal investigator · StLukesNY

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2015. You cannot join it, but the record below documents what was studied.

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