A Pilot Feasibility Trial of Nasogastric fluid Options in BROnchiolitis: The NOBRO study

Not Applicable

Completed

• Conditions: Bronchiolitis; Respiratory - Other respiratory disorders / diseases; Infection - Other infectious diseases

• Registration Number: ACTRN12619001789156
• Lead Sponsor: Gold Coast University Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-12-19
• Study Completion: 2020-12-20
• Last Update Posted: 20 September 2021

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 32

Inclusion Criteria

•Inclusion criteria
oPatient under 12 months (and 0 days) chronological age
oPatient diagnosed with bronchiolitis (regardless of the severity) as their primary diagnosis for hospital admission
oPatient deemed by their treating clinician to require nasogastric fluids due to poor oral feeding

Exclusion Criteria

1. Nasogastric tube, or other gastric feeding device in situ already in situ for normal feeds in the pre-morbid state
2. Requiring > 2L/kg of Highflow oxygen at the time of initiating nasogastric fluids
3. Receiving non invasive mask ventilation (CPAP or BIPAP) at the time of initiating nasogastric fluids
4. Intubated and requiring mechanical ventilation at the time of initiating nasogastric fluids
High clinical suspicion of the need for escalated respiratory support (ie. Above 2L/kg of highflow oxygen) within the next 24 hours
5. Patients transferred to Gold Coast University Hospital from a peripheral hospital, or with a plan for backtransfer to a peripheral hospital

Study & Design

• Study Type: Interventional
• Study Design: Not specified