Overview

Measurement of Respiratory Admittance for Pediatric Asthma Diagnosis

Status:
Completed
Trial end date:
2012-04-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose is to characterize the change of respiratory admittance induced by salbutamol inhalation in children and young adults. A variation threshold will be fixed to distinguish asthmatic and healthy subjects. This project could allow a better identification of asthmatic individuals needing a treatment, a reduction of morbidity of asthma, a reduction of unnecessary treatments administered in individuals with respiratory but not asthmatic symptoms, a better comprehension of bronchial hyperreactivity and its role in asthmatic disease.
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Central Hospital, Nancy, France
Treatments:
Albuterol
Criteria
Inclusion Criteria:

Asthmatic children group:

- Several episodes of paroxysmal wheezes, spontaneous or after exercise, without
bronchial-pulmonary infection

- Absence of bronchodilator taking during last 12 hours

- Absence of reported intolerance to adrenergic substances

- Parental authorization and consent of child to participate to the study

Control children group:

- Parental authorization and consent of child to participate to the study

Control adult group:

- Consent to participate to the study

Exclusion Criteria:

Control children and adult groups:

- At least 2 episodes of wheezes during breathing

- Several wheezes, abnormal breathlessness, cough during physical exercise

- Asthma diagnosed by family doctor

- Administration of drugs to treat asthma

- Eczema or food allergy at inclusion

- Episode of cough for longer than 6 weeks, without bronchial infection

- Bronchitis, throat infection, rhino-pharyngitis during last 15 days

- Paleness or cyanosis with loss of consciousness when the child was a baby or during an
exercise