Clinical Trials Directory

Trials / Completed

CompletedNCT06558461

Nebulised 3% Hypertonic Saline in Infants With Acute Bronchiolitis

Evaluating the Efficacy of Nebulised 3% Hypertonic Saline for Acute Bronchiolitis in Infants: A Study at Can Tho Children's Hospital, 2022-2024

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
140 (actual)
Sponsor
Can Tho University of Medicine and Pharmacy · Academic / Other
Sex
All
Age
1 Month – 24 Months
Healthy volunteers
Not accepted

Summary

This study aims to determine the efficacy of nebulising 3% hypertonic saline in improving clinical symptoms and reducing the length of hospital stay in infants with acute bronchiolitis.

Detailed description

Bronchiolitis is the most prevalent disease in infants, especially children younger than two years old. Clinical manifestations vary from mild to severe, even life-threatening respiratory failure. Airway oedema and mucus plugging are the principal pathological features in infants with acute bronchiolitis. Nebulising 3% hypertonic saline solution may reduce these pathological changes, but the evidence remains equivocal.

Conditions

Interventions

TypeNameDescription
DRUG3% Sodium Chloride4ml nebulized three times daily
OTHERStandard careStandard care

Timeline

Start date
2022-06-01
Primary completion
2024-05-27
Completion
2024-05-28
First posted
2024-08-16
Last updated
2024-08-16

Locations

1 site across 1 country: Vietnam

Regulatory

Source: ClinicalTrials.gov record NCT06558461. Inclusion in this directory is not an endorsement.