Efficacy of High-Dose Continuous Intravenous Magnesium Sulfate Infusion vs Standard Intravenous Magnesium Sulfate Therapy in Status Asthmaticus in the ED

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorThammasat University

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • ้High-dose Magnesium sulphate

    Drug

    Participants 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

    Drug

    Participants 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

72 Participants
are divided into 2 treatment groups
Group A: High dose MgSO4 Continuous IV dripExperimental treatment 2 interventions
Group B: standard-dose MgSO4 Continuous IV dripActive comparator 2 interventions

Trial outcomes

Primary outcomes

1

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.

Time frame
through study completion, an average of 1 year

Secondary outcomes

1

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.

Time frame
through study completion, an average of 1 year

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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