About this trial
The goal of this clinical is to compare treatment outcomes between high dose continuous IV Magnesium and standard therapy in the management of acute exacerbation of asthma in the emergency department. Participants will random assign to either high dose continuous IV drip or standard infusion. Participants in the intervention group received high-dose 50% magnesium sulfate (MgSO4), consisting of 2 g + normal saline (NSS) 100 ml administered intravenously over 30 minutes, followed by MgSO4 6 g + NSS 350 ml infused over 3.5 hours (approximately 40-50 mg/kg/h). In contrast, participants in the control group received standard-dose 50% MgSO4, consisting of 2 g + NSS 100 ml administered intravenously over 30 minutes, followed by a NSS 350 ml infusion over 3.5 hours. 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.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Adults aged ≥18 years with a known diagnosis of asthma, and
Presence of signs and symptoms consistent with acute asthma exacerbation, including dyspnea, tachypnea, respiratory distress, chest tightness, cough, or wheezing, and
Indication for administration of intravenous magnesium sulfate (MgSO4)
Disqualifiers
Patients requiring endotracheal intubation at the time of initial presentation
Hypermagnesemia (more than 2.5 mg/dL)
Known hypersensitivity to magnesium sulfate
Diagnosed or suspected myasthenia gravis or neuromuscular disease
Trial design
Parallel
Treatments tested in this trial
้High-dose Magnesium sulphate
DrugParticipants in the intervention group received high-dose 50% magnesium sulfate (MgSO₄), consisting of 2 g diluted in 100 mL normal saline (NSS) administered intravenously over 30 minutes, followed by MgSO₄ 6 g diluted with NSS up to a total volume of 350 mL infused intravenously over 3.5 hours (approximately 40-50 mg/kg/h).
standard-dose Magnesium Sulfate
DrugParticipants in the control group received standard-dose 50% MgSO₄, consisting of 2 g diluted in 100 mL NSS administered intravenously over 30 minutes, followed by 350 mL NSS infused over 3.5 hours
Treatment groups
Trial outcomes
Primary outcomes
Length of ED stay (hours)
Length of ED stay was defined as the time from administration of the first nebulized treatment to the time of physician-ordered disposition from the emergency department.
Secondary outcomes
Hospital admission rate (%)
Hospital admission rate (%) was defined as admission to an inpatient ward or intensive care unit directly from emergency department following the index visit.
Locations
Sponsors and contacts
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