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Continuous Versus Intermittent Nebulization Therapy in Acute Asthma Exacerbation at Emergency Department

Emergency Department Clinical Trial

Official title:
Continuous Versus Intermittent Nebulization Therapy in Acute Asthma Exacerbation at Emergency Department: A Randomized Controlled Trial

Clinical Trial Summary

The goal of this clinical is to compare treatment outcomes between continuous nebulization and intermittent therapy in the management of acute exacerbation of asthma in the emergency department(ED). Participants will random assign to either continuous or intermittent nebulization. In the continuous group, patients receive budesonide, fenoterol, ipratropium bromide, and normal saline continuously for an hour. In the intermittent group, the same medications are administer every 20 minutes for an hour. Measurements include symptom severity, respiratory rate, oxygen saturation, and pulmonary function tests. Primary endpoints are ED stay length, hospital admission, and ED revisit within 48 hours post-discharge. Adverse events are documented.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06291740
Study type Interventional
Source Thammasat University
Contact Kumpol Kornthatchapong, Assoc.Prof.
Phone +66954951555
Email kump29@gmail.com
Status Not yet recruiting
Phase N/A
Start date April 2024
Completion date May 2025
View Details
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