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
| Type | Name | Description |
|---|---|---|
| DRUG | 3% Sodium Chloride | 4ml nebulized three times daily |
| OTHER | Standard care | Standard 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
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT06558461. Inclusion in this directory is not an endorsement.