COAST (Childhood Origins of ASThma)
Recruitment status was Active, not recruiting
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Purpose
Although asthma is likely to be a heterogeneous disease or syndrome, three factors and/or events repetitively emerge for their ability to significantly influence asthma inception in the first decade of life: immune response aberrations, which appear to be defined best by the concept of cytokine dysregulation; lower respiratory tract infections (in particular RSV); and some form of gene by environment interaction that needs to occur at a critical time period in the development of the immune system or the lung. It remains to be firmly established, however, how any one or all of these factors, either independently or interactively, influence the development of childhood asthma. Thus, our efforts to determine and define the importance of these three factors to asthma pathogenesis are the focus and goal of this current grant application.
| Condition |
|---|
|
Childhood Asthma |
| Study Type: | Observational |
| Study Design: | Observational Model: Defined Population Time Perspective: Longitudinal Time Perspective: Prospective |
| Official Title: | Cytokine Dysregulation, Virus Infection, and Asthma: The Pathogenesis of Childhood Asthma |
Eligibility| Ages Eligible for Study: | up to 2 Minutes |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- children who had one or more parent with a history of allergy or asthma
Exclusion Criteria:
-
Contacts and Locations| United States, Wisconsin | |
| University of Wisconsin | |
| Madison, Wisconsin, United States, 53792 | |
| Principal Investigator: | Robert F Lemanske, Jr., MD | University of Wisconsin, Madison |
More Information
Additional Information:
No publications provided
| ClinicalTrials.gov Identifier: | NCT00204841 History of Changes |
| Other Study ID Numbers: | 1998-129, R01 HL61879, P01 HL70831 |
| Study First Received: | September 12, 2005 |
| Last Updated: | September 13, 2005 |
| Health Authority: | United States: Food and Drug Administration |
Additional relevant MeSH terms:
|
Asthma Bronchial Diseases Respiratory Tract Diseases Lung Diseases, Obstructive Lung Diseases |
Respiratory Hypersensitivity Hypersensitivity, Immediate Hypersensitivity Immune System Diseases |
ClinicalTrials.gov processed this record on May 22, 2013