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The Impact of Treating Staphylococcus Aureus Infection and Colonization on the Clinical Severity of Atopic Dermatitis

This study has been completed.
Sponsor:
Collaborators:
Society for Pediatric Dermatology
Johnson & Johnson
Information provided by (Responsible Party):
Amy Paller, Northwestern University
ClinicalTrials.gov Identifier:
NCT00179959
First received: September 13, 2005
Last updated: November 29, 2012
Last verified: October 2012
History of Changes
Results First Received: April 4, 2011  
Study Type: Interventional
Study Design: Allocation: Randomized;   Endpoint Classification: Safety/Efficacy Study;   Intervention Model: Parallel Assignment;   Masking: Double Blind (Subject, Investigator);   Primary Purpose: Treatment
Condition: Atopic Dermatitis
Interventions: Drug: Sodium hypochlorite (bleach) baths
Drug: Mupirocin ointment
Drug: Water
Drug: Petrolatum Ointment

  Participant Flow
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Recruitment Details
Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
Patients were recruited from Children's Memorial Hospital's pediatric dermatology clinic.

Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
No text entered.

Reporting Groups
  Description
Treatment Intranasal mupirocin ointment treatment and sodium hpochlorite (bleach baths)
Placebo Intranasal petrolatum ointment treatment and plain water baths

Participant Flow:   Overall Study
    Treatment     Placebo  
STARTED     15     16  
COMPLETED     9     13  
NOT COMPLETED     6     3  
Lost to Follow-up                 3                 1  
Withdrawal by Subject                 3                 2  



  Baseline Characteristics
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Reporting Groups
  Description
Treatment Intranasal mupirocin ointment treatment and sodium hpochlorite (bleach baths)
Placebo Intranasal petrolatum ointment treatment and plain water baths
Total Total of all reporting groups

Baseline Measures
    Treatment     Placebo     Total  
Number of Participants  
[units: participants]
 		  15     16     31  
Age  
[units: participants]
 		     
<=18 years     15     16     31  
Between 18 and 65 years     0     0     0  
>=65 years     0     0     0  
Gender  
[units: participants]
 		     
Female     8     8     16  
Male     7     8     15  
Region of Enrollment  
[units: participants]
 		     
United States     15     16     31  



  Outcome Measures

1.  Primary:   Change in Eczema Area and Severity Index (EASI)Scores According to Location   [ Time Frame: Baseline and 3 months ]
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  Serious Adverse Events
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  Other Adverse Events
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  More Information
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