Status:

COMPLETED

The Underlying Mechanisms For S. Aureus Infection And Colonization Of Skin in People With Atopic Dermatitis With And Without Eczema Herpeticum (MRSA)

Lead Sponsor:

National Institute of Allergy and Infectious Diseases (NIAID)

Conditions:

Methicillin-Resistant Staphylococcus Aureus

Atopic Dermatitis

Eligibility:

All Genders

1-80 years

Brief Summary

Staphylococcus aureus (S.aureus) is a bacterium that causes many painful skin and soft tissue conditions, such as scalded-skin syndrome, boils, or impetigo. Serious cases may result in deadly complica...

Detailed Description

The emergence of drug-resistant staphylococcal strains was first seen in the US almost a decade ago, when the Centers for Disease Control (CDC) reported four fatal community-based MRSA infections in c...

Eligibility Criteria

Inclusion

  • Parent, or legal guardian willing to provide informed consent, if necessary
  • Residing in the U.S.
  • Have active AD with or without a history of EH as diagnosed using the ADVN Standardized Diagnostic Criteria OR are non-atopic as diagnosed using the ADVN Standardized Diagnostic Criteria

Exclusion

  • History of any systemic illness (i.e., immunodeficiency disorders such as human immunodeficiency virus \[HIV\] or lupus erythematosus) other than the condition being studied
  • Presence of active systemic malignancy, excluding uncomplicated non-melanoma skin cancer
  • Presence of any skin disease other than AD that might compromise the stratum corneum barrier (e.g., bullous disease, psoriasis, cutaneous T cell lymphoma \[also called Mycosis Fungoides or Sezary syndrome\])
  • Use of topical medications including (but not limited to) Elidel, Protopic, or topical corticosteroids at the site of the skin lesion within the last 3 days
  • Use of topical antibiotics within the last 24 hours
  • Use of oral antibiotics within the last 10 days. Subjects who are known to be culture positive for MSSA or MRSA despite antibiotic treatment will not be excluded.
  • History of serious or life-threatening reactions to tape or adhesives will be excluded from the tape stripping procedure

Key Trial Info

Start Date :

February 1 2009

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

November 1 2009

Estimated Enrollment :

65 Patients enrolled

Trial Details

Trial ID

NCT00822276

Start Date

February 1 2009

End Date

November 1 2009

Last Update

April 4 2014

Active Locations (2)

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Page 1 of 1 (2 locations)

1

University of California, San Diego

San Diego, California, United States, 92161

2

National Jewish Health

Denver, Colorado, United States, 80206