Last updated: March 17, 2024
Sponsor: Kuopio University Hospital
Overall Status: Active - Recruiting
Phase
N/A
Condition
Respiratory Syncytial Virus (Rsv) Infection
Bronchitis (Pediatric)
Treatment
High flow nasal cannula weaning
High flow nasal cannula immediate ending
Clinical Study ID
NCT06321133
5402589
Ages < 12 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- 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
Exclusion
Exclusion Criteria:
- Major congenital anomaly of lungs, hearts or diaphragm
- Bacterial pneumonia
- Parents do not give consent
Study Design
Total Participants: 50
Treatment Group(s): 2
Primary Treatment: High flow nasal cannula weaning
Phase:
Study Start date:
February 13, 2024
Estimated Completion Date:
December 31, 2026
Study Description
Connect with a study center
Siun Sote
Joensuu,
FinlandActive - Recruiting
Central Finland Hospital District
Jyväskylä,
FinlandActive - Recruiting
Kuopio University Hospital
Kuopio,
FinlandActive - Recruiting
Mikkeli Central Hospital
Mikkeli,
FinlandActive - Recruiting
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