Status:

COMPLETED

Role of Antimicrobial Peptides in Host Defense Against Vaccinia Virus

Lead Sponsor:

National Institute of Allergy and Infectious Diseases (NIAID)

Conditions:

Atopic Dermatitis

Eligibility:

All Genders

2+ years

Brief Summary

Atopic dermatitis (AD) is a chronic inflammatory skin disorder characterized by recurrent viral skin infections. Recent studies have demonstrated that the skin of people with AD my have decreased anti...

Detailed Description

AD is a chronic inflammatory skin disease characterized by frequent viral skin infections. Recent studies have found that components in the skin of people with AD may block AMP expression. AMPs are re...

Eligibility Criteria

Inclusion

  • Inclusion Criteria for Participants With AD:
  • 2 years of age or older
  • History of active or inactive AD OR eczema herpeticum, as defined by the ADVN standardized diagnostic criteria
  • Parent or guardian willing to provide informed consent, if applicable
  • Male or female of any race and ethnicity
  • Inclusion Criteria for Participants With Asthma or Psoriasis, and for non-atopic controls:
  • 18 years or older
  • History of psoriasis OR history of asthma not requiring systemic medications
  • Parent or guardian willing to provide informed consent, if applicable
  • Male or female of any race and ethnicity
  • Exclusion Criteria:
  • Oral corticosteroids or any systemic immunosuppressive or immunomodulatory medication within 28 days prior to study entry
  • Immunotherapy within 3 months prior to study entry
  • History of bleeding disorder
  • Aspirin, oral antihistamines, oral antibiotics, oral cyclosporine, or topical medications within 7 days of screening visit including, but not restricted to, Protopic, Elidel, topical corticosteroids, and topical antibiotics
  • Anxiolytic agents and antidepressants within 2 days of screening visit
  • Diabetic requiring medication
  • Autoimmune or immunodeficiency
  • Active fungal, bacterial, or viral infections within 7 days prior to study entry
  • Active systemic cancer. Participants with uncomplicated nonmelanoma skin cancer are not excluded.
  • Theophylline or leukotriene antagonists within 24 hours of screening visit
  • Received any vaccination within 30 days prior to study entry
  • Known lidocaine allergy
  • Previously vaccinated for smallpox
  • Pregnant or breastfeeding

Exclusion

    Key Trial Info

    Start Date :

    June 1 2005

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ACTUAL

    End Date :

    February 1 2010

    Estimated Enrollment :

    286 Patients enrolled

    Trial Details

    Trial ID

    NCT00407069

    Start Date

    June 1 2005

    End Date

    February 1 2010

    Last Update

    October 18 2016

    Active Locations (1)

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    National Jewish Health

    Denver, Colorado, United States, 80207