Skip to content

Canadian Bronchiolitis Epinephrine Steroid Trial

A randomised controlled trial of nebulised epinephrine and oral dexamethasone in the treatment of outpatients with bronchiolitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN56745572
Enrollment
800
Registered
2005-09-26
Start date
2004-04-01
Completion date
Unknown
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bronchiolitis Respiratory Bronchiolitis

Interventions

1. Oral dexamethasone 2. Nebulised epinephrine Trial details received: 12 Sept 2005

Sponsors

Children's Hospital of Eastern Ontario (Canada)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age 6 weeks to 12 months, either sex 2. Respiratory distress assessment instrument (RDAI) score of greater than 3 and less than 15 3. Diagnosis of bronchiolitis

Exclusion criteria

Exclusion criteria: 1. Asthma or any previous episode of wheezing treated with bronchodilators 2. Chronic cardiopulmonary disease 3. Presence of varicella or recent close contact 4. Severe respiratory distress 5. Recent treatment with oral or inhaled steroids 6. Insurmountable language barrier 7. Any child born at less than 37 weeks gestation who is less than 6 weeks corrected age

Design outcomes

Primary

MeasureTime frame
Admission to hospital up to 7 days after enrolment

Secondary

MeasureTime frame
1. Time to discharge 2. Length and severity of symptoms 3. Change in RDAI 4. Economic costs 5. Change in oxygen saturation from baseline at times 60, 120, 180 and 240 minutes 6. Co-interventions 7. Return to be evaluated by health care provider for on-going symptoms related to bronchiolitis 8. Adverse events

Countries

Canada

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 3, 2026