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The Natural Course of Trichophyton Tonsurans Carriage and Infection: A Molecular and Biochemical Evaluation

This study has been completed.

Sponsored by: National Institute of Child Health and Human Development (NICHD)
Information provided by: National Institute of Child Health and Human Development (NICHD)
ClinicalTrials.gov Identifier: NCT00224926
  Purpose

To explore carrier and infection status of T.tonsurans tinea capitis and characterize the host-pathogen interaction as it relates to the disease presentation. The general hypothesis for this study is as follows: the type of genotypic and phenotypic variant to which a child is exposed accounts for the presentation status observed in Trichophyton tonsurans infection.The global outcome of this investigation is to reveal potential new drug targets designed to improve treatment outcomes in these children.


Condition Intervention
Tinea Capitis
Procedure: Scalp Brushing

MedlinePlus related topics:   Tinea Infections   

U.S. FDA Resources

Study Type:   Observational
Study Design:   Natural History, Longitudinal, Random Sample
Official Title:   The Natural Course of Trichophyton Tonsurans Carriage and Infection: A Molecular and Biochemical Evaluation

Further study details as provided by National Institute of Child Health and Human Development (NICHD):

Estimated Enrollment:   350
Study Start Date:   September 2003
Estimated Study Completion Date:   September 2005

Detailed Description:

Tinea capitis is an overwhelmingly prevalent disease of childhood estimated to be present in approximately 1 in 20 children at any point in time with an equal number of children serving as carriers of the fungal pathogen. Despite the widespread nature of the disease, the natural course of the infection remains incompletely described. The study will be driven by the following hypothesis:the type of genotypic and phenotypic variant to which a child is exposed accounts for the presentation status observed in Trichophyton tonsurans infection.

A fungal scalp culture will be acquired from all participants using a brush culture technique. Samples will be collected once a month over a two year time period.

  Eligibility
Ages Eligible for Study:   2 Years to 5 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes

Criteria

Inclusion Criteria:

  • Preschool aged children will be eligible.

Exclusion Criteria:

  • None
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00224926

Locations
United States, Missouri
Children's Mercy Hospital    
      Kansas City, Missouri, United States, 64108

Sponsors and Collaborators
  More Information

Pediatric Pharmacology Research Unit Website  This link exits the ClinicalTrials.gov site
 

Study ID Numbers:   PPRU 10704
First Received:   September 21, 2005
Last Updated:   April 9, 2007
ClinicalTrials.gov Identifier:   NCT00224926
Health Authority:   United States: Federal Government

Keywords provided by National Institute of Child Health and Human Development (NICHD):
Tinea Capitis  

Study placed in the following topic categories:
Mycoses
Skin Diseases, Infectious
Skin Diseases
Tinea Capitis
Tinea
Dermatomycoses

Additional relevant MeSH terms:
Scalp Dermatoses
Infection

ClinicalTrials.gov processed this record on September 04, 2008




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