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临床试验/NCT00515047
NCT00515047已完成不适用

Genetics of Atopic Dermatitis - Eczema Herpeticum

National Institute of Allergy and Infectious Diseases (NIAID)7 个研究点 分布在 1 个国家目标入组 900 人开始时间: 2006年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
900
试验地点
7
主要终点
Identification of variants/haplotypes in EH-associated genes and characterization of frequencies of variants in priority candidate genes for EH

研究概览

简要总结

People with atopic dermatitis (AD), or eczema, are susceptible to skin infections and inflammations. Some individuals with AD develop a condition known as eczema herpeticum (EH) following exposure to the herpes simplex virus (HSV). The purpose of this study is to identify the genetic determinants that lead people with AD to develop EH and similar conditions caused by other viruses.

详细描述

AD is a chronic inflammatory skin disorder characterized by recurrent viral skin infections. However, people with AD do not all develop the same infections. For example, some people with AD who receive the smallpox vaccine develop a life-threatening condition known as eczema vaccinatum (EV). This study focuses on individuals with AD who also have a history of eczema herpeticum (ADEH+), a condition similar to EV. It is unlikely that the differences in the development of skin infections are due to differences in viral exposure, and instead due to differences in each individual's response to viruses. The purpose of this study is to determine the genetic pathways which are responsible for the development of viral skin infections in people with AD.

Participants in this study will also be enrolled in the ADVN Biomarker Registry Study. There will be only one clinical visit for this study at which blood and/or skin samples may be collected. The samples will then have high-throughput genotyping to define genetic markers in individuals susceptible to viral infections.

研究设计

研究类型
Observational
时间视角
Cross Sectional

入排标准

年龄范围
8 Months 至 80 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Enrollment in ADVN Biomarker Registry Study
  • Non-Hispanic and only African American or only Caucasian race
  • Parent or guardian willing to provide informed consent, if necessary

排除标准

  • History of any systemic illness, excluding AD
  • Participation of a first degree relative already enrolled in the genotyping study unless the subject in question fulfills the diagnostic criteria for ADEH+. More information on this criterion can be found in the protocol.

结局指标

主要结局

Identification of variants/haplotypes in EH-associated genes and characterization of frequencies of variants in priority candidate genes for EH

时间窗: Throughout Study

次要结局

  • Identification and prioritization of novel genes induced in response to viral infection (HSV/Vaccinia and MCV) in AD participants and relevant control groups(Throughout Study)

研究者

申办方类型
Nih
责任方
Sponsor

研究点 (7)

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