Completed
COASTRhinovirus Infection and Asthma in Childhood and Adolescents
What is being collected
Data Collection
Collected from today forward - ProspectiveDNA Samples
Who is being recruted
Asthma+6
+ Bronchial Diseases
+ Hypersensitivity
+4 Eligibility Criteria
How is the trial designed
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Observational
Study Start: October 1998
Summary
Principal SponsorUniversity of Wisconsin, Madison
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner
Study start date: October 1, 1998
Actual date on which the first participant was enrolled.No more description necessary.
Official TitleRhinovirus Infection and Asthma in Childhood and Adolescents
Principal SponsorUniversity of Wisconsin, Madison
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Design Details
287 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Conditions
Criteria
Any sex
Biological sex of participants that are eligible to enroll.Range of ages for which participants are eligible to join.
Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
AsthmaBronchial DiseasesHypersensitivityHypersensitivity, ImmediateImmune System DiseasesLung DiseasesLung Diseases, ObstructiveRespiratory HypersensitivityRespiratory Tract Diseases
Criteria
1 inclusion criteria required to participate
children who had one or more parent with a history of allergy or asthma
3 exclusion criteria prevent from participating
pre term infants
low birth weight infants
respiratory distress at birth
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Study Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Suspended
CompletedOne Study Center