High Flow Nasal Cannula Weaning in Acute Bronchiolitis
Recruiting now · Not applicable
Conditions studied: Acute Bronchiolitis
In brief
The goal of this clinical study is to compared two different strategies to end high flow nasal cannula treatment in acute bronchiolitis. This study compared the immediate ending of high flow treatment to weaning strategy, in which the flow rate is gradually decreased. The aim is to assess if the immediate ending shortens the hospitalization time and whether it is a safe strategy.
Key facts
- Study ID
- NCT06321133
- Run by
- Kuopio University Hospital
- People needed
- 50
- Starts
- 2024-02-13
- Expected to finish
- 2028-12-31
- Last updated by the study team
- 2025-09-03
Who can join
Age: any, up to 1. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Clinically diagnosed acute bronchiolitis
- High flow nasal cannula treatment has lasted for at least 12 hours
- Measured saturation 95 or more with room air
- High flow rate is maximum 2l/kg/min
- The treating doctors considers the infant suitable to be without high flow
You may not qualify if…
- Major congenital anomaly of lungs, hearts or diaphragm
- Bacterial pneumonia
- Parents do not give consent
Where it is running
- Siun Sote — Joensuu, Finland (enrolling)
- Central Finland Hospital District — Jyväskylä, Finland (enrolling)
- Kuopio University Hospital — Kuopio, Finland (enrolling)
- Mikkeli Central Hospital — Mikkeli, Finland (enrolling)
Full record on ClinicalTrials.gov
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