Phase
Condition
Respiratory Syncytial Virus (Rsv) Infection
Bronchitis (Pediatric)
Asthma
Treatment
N/AClinical Study ID
Ages 2-12 All Genders
Study Summary
Eligibility Criteria
Inclusion
INCLUSION CRITERIA
Parent/Guardian able to provide written informed consent
Within 6 weeks of discharge from hospital following admission for bronchiolitis
Child aged is ≥2 weeks of age and ≤ 12 months on the date of hospital admission for Bronchiolitis
A diagnosis of Bronchiolitis requiring a hospital admission (defined as more than 4 hours in hospital)
Contactable for regular follow up by the research team
EXCLUSION CRITERIA
Any previous hospital attendance for bronchiolitis
More than one episode of healthcare professional-diagnosed wheeze prior to index bronchiolitis episode
Premature gestational age less than 34 weeks
Any severe chronic condition such as cystic fibrosis, sickle cell disease, severe developmental delay, immunodeficiency, or anything that has a significant impact on the respiratory tract (such as need for non-invasive ventilation) or increases vulnerability to respiratory tract infections.
History of clinically significant neonatal disease (e.g. neonatal pneumonia, congenital lung abnormality, neonatal chronic lung disease)
Genetic conditions that affect the immune system (e.g. Down's syndrome/Trisomy 21)
Current regular oral montelukast or inhaled corticosteroid therapy or inhaled salbutamol therapy
Current regular treatment with immunomodulatory drugs (e.g oral steroids)
Known allergy or previous intolerance to study medication.
Enrolment in another clinical trial of a medicinal product. Non-CTIMP study participation is allowed.
Sibling of a BLIPA participant (of the same household or family)
Study Design
Study Description
Connect with a study center
Barts Health NHS Trust
London,
United KingdomActive - Recruiting
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