Clinical trial

Nebulised 3% Hypertonic Saline Versus 0.9% Saline for Treating Patients Hospitalized With Acute Bronchiolitis: Protocol of a Randomized, Double-blind, Multicentre Trial

Name
1/2023
Description
Bronchiolitis is an acute viral infection of the lower respiratory tract. It is most commonly caused by respiratory syncytial virus (RSV). Only supportive therapy, including suctioning nasal secretions, water-electrolyte balance maintenance, and oxygen supplementation when needed, is recommended. The inhalation of 3% hypertonic saline is not recommended in bronchiolitis management. However, a recently published meta-analysis revealed that the inhalation of hypertonic saline can reduce the risk of hospitalisation for outpatients with bronchiolitis, while resulting in a shorter length of hospital stay and reduced severity of respiratory distress for inpatients, although the evidence is of low certainty. The aim of the study is to assess the efficacy of nebulised hypertonic saline for the treatment of children hospitalised with bronchiolitis.
Trial arms
Trial start
2023-11-01
Estimated PCD
2025-03-01
Trial end
2025-03-01
Status
Recruiting
Treatment
Hypertonic saline
Nebulised 3% hypertonic saline (NEBU-dose hypertonic). Nebulisation will be performed by trained study nurses or by parents under the supervision of a nurse
Arms:
Hypertonic saline
Normal saline
0,9% normal saline (NEBU-dose isotonic). Nebulisation will be performed by trained study nurses or by parents under the supervision of a nurse
Arms:
Normal saline
Size
140
Primary endpoint
Length of hospital stay (LOS).
From admission to hospital discharge
Eligibility criteria
Inclusion Criteria: 1. Children admitted to the hospital with the clinical diagnosis of acute bronchiolitis, which is defined as an apparent viral respiratory tract infection associated with airway obstruction manifested by at least one of following symptoms: * Tachypnoea (WHO definition). * Increased respiratory effort manifested as follows: 1. Nasal flaring; 2. Grunting; 3. Use of accessory muscles; 4. Intercostal and/or subcostal chest wall retractions; 5. Apnoe. * Crackles and/or wheezing. 2. Aged 5 weeks - 24 months old. 3. A caregiver must provide written informed consent. Exclusion Criteria: 1. Infants hospitalised with severe bronchiolitis (requiring mechanical ventilation or intensive care, or oxygen saturation \< 85% on room air). 2. History of prematurity (gestational age \<34 weeks). 3. Diagnosis of a clinically significant chronic disease (cardiac, respiratory, neuromuscular, or metabolic). 4. Immunodeficiency. 5. Gastro-oesophageal reflux. 6. Diagnosis or suspicion of asthma. 7. Inhaling a nebulised 3% hypertonic saline solution within 12 hours before enrolment. 8. Inhaling bronchodilators within 24 hours before enrolment. 9. Inhaling steroids within 24 hours before enrolment. 10. Systemic steroid therapy in the preceding 2 weeks.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['NA'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'interventionModelDescription': 'Randomization will occur within 24 hours of admission', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 140, 'type': 'ESTIMATED'}}
Updated at
2023-11-28

1 organization

2 products

1 indication

Indication
Bronchiolitis