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Clinical Trials/ISRCTN58244066
ISRCTN58244066
Completed
Not Applicable

Asthma Reduction with Inhaled corticoSteroids in Children with a high risk for the development of asthma (At RISC)

Care and Public Health Research Institute (CAPHRI), University Maastricht (Netherlands)0 sites97 target enrollmentJanuary 27, 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Care and Public Health Research Institute (CAPHRI), University Maastricht (Netherlands)
Enrollment
97
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 27, 2006
End Date
TBD
Last Updated
11 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Care and Public Health Research Institute (CAPHRI), University Maastricht (Netherlands)

Eligibility Criteria

Inclusion Criteria

  • 1\. Male and female patients aged 1\-4\.5 years with a familial predisposition for asthma in the first degree, who have experienced at least 2 separate periods with wheeze lasting at least 2 days each documented by their general practitioner
  • 2\. For each patient who enters the study a written informed consent by the parent or guardian of the patient should be obtained

Exclusion Criteria

  • 1\. Patients who have been treated with pulmonary anti\-inflammatory inhaled drugs for more than 2 weeks or anti\-inflammatory oral drugs for more than 1 week preceding the study
  • 2\. Patients who have been hospitalised for asthma in the 2 weeks prior to the study
  • 3\. Patients who have serious respiratory morbidity (e.g. broncho\-pulmonary dysplasia, cystic fibrosis, tuberculosis)
  • 4\. Patients, who have laboratory or clinical evidence of serious uncontrolled systemic disease (as judged by the investigator)
  • 5\. Patients with anatomical abnormalities of the upper airways or lungs
  • 6\. Patients currently participating in another drug intervention study
  • 7\. When the general practitioner considers it detrimental to the patient to participate in the study

Outcomes

Primary Outcomes

Not specified

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