Salbutamol in the Pediatric Emergencies: Nebulization Estimated Via AerogeN or Jet (SIBILANT)
Asthma
About this trial
This is an interventional device feasibility trial for Asthma focused on measuring pediatrics, asthma, nebulization, vibrating mesh, salbutamol, Efficiency
Eligibility Criteria
Inclusion Criteria:
- Children aged 8-16 years.
- Patient with severe asthma (maximum expiratory flow <50%).
- Patient admitted to pediatric emergency.
- Patient who has agreed to participate, as well as the parents or legal guardian.
Exclusion Criteria:
Chronic respiratory failure, infectious disease, heart disease.
- Refusal to participate in the study.
- No affiliation to a social security scheme (beneficiary or beneficiary).
- Immediate intubation criteria
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
vibrating Mesh nebulizer
jet nebulizer
Receive in the same aerosol solution 5 mg of Salbutamol (Ventolin, Glaxo, 5 mg / ml solution for nebulization) mixed with 0.5 mg Ipratropium Bromide (0.25 mg / ml) by nebulization every 20 min For 3 doses during the first hour of treatment, using vibrating Mesh nebulizer
Receive, in the same aerosol solution, 5 mg of Salbutamol (Ventolin, Glaxo, 5 mg / ml solution for nebulization) mixed with 0.5 mg Ipratropium Bromide (0.25 mg / ml) by nebulization every 20 min For 3 doses during the first hour of treatment, using a jet nebulizer