Magnesium sulfate for treating exacerbations of acute asthma in the emergency department.
B H Rowe, J A Bretzlaff, C Bourdon...
https://pubmed.ncbi.nlm.nih.gov/10796650/Actively Recruiting
Led by University of Oklahoma · Updated on 2024-12-06
100
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are evaluating whether giving intravenous magnesium sulfate early in moderate asthma attacks can reduce hospital admissions, shorten the time spent in the emergency department and hospital, and lessen the need for breathing support in children aged 5 to 17. This study focuses on moderate asthma exacerbations and aims to compare early magnesium treatment with standard care to understand its potential benefits. The research is conducted by the University of Oklahoma and involves children presenting at a hospital emergency department with a moderate respiratory score. Participants are randomly assigned to one of two groups after consent one group receives a weight-based dose of IV magnesium sulfate within the first hour of treatment alongside standard asthma therapies such as inhaled beta agonists and IV steroids. The dosing varies by weight, ranging from 750 mg to 2000 mg. The other group does not receive magnesium sulfate within the first hour but may be given it later if deemed necessary by the provider. Both groups will be monitored throughout their hospital stay. During the study, patients clinical progress will be tracked, including length of stay in the emergency department and hospital, the need for respiratory support, and pediatric intensive care unit stay if applicable. Researchers will collect data up to one week for length of stay outcomes and up to two weeks for respiratory support needs. The study runs from late 2023 to mid-2024 and includes assessments of the impact of early magnesium treatment on asthma exacerbation management in children.
CONDITIONS
Timely Administration of IV Magnesium Sulfate in Patients With a Moderate Asthma Exacerbation
R
Ryan McKee, MD
J
Jaclyn Urquiola Sorzano, DO
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University of Oklahoma
Lead Sponsor
This table compares participation in this trial with other options available for this condition. The information is drawn from published research and the trial’s study details and is provided for educational purposes only.
| Factors | IV Magnesium Sulfate (Early Administration) | Usual Asthma Therapies (No Early Magnesium) |
|---|---|---|
| What it is | Children receive intravenous magnesium sulfate (40-50 mg/kg, adjusted for weight) in the first hour in addition to standard asthma treatments such as inhaled beta agonists and IV steroids. | Children are treated with usual asthma therapies (inhaled beta agonists, IV steroids) and do not receive intravenous magnesium sulfate within the first hour. |
| Role in trial | Investigational intervention; assesses whether early IV magnesium added to standard care improves outcomes in moderate pediatric asthma exacerbations. | Active comparator; follows current standard therapies for moderate pediatric asthma attacks without IV magnesium in the first hour. |
| Primary use | Studied as an adjunct treatment to relieve moderate asthma attacks and potentially shorten emergency department stay. | Established first-line therapies (inhaled beta agonists, IV steroids) used to manage moderate asthma attacks. |
| How it is given or performed | Administered intravenously (40-50 mg/kg based on actual body weight) with a 20 mL/kg saline bolus during the first hour of care. | Does not receive IV magnesium sulfate; receives inhaled beta agonists and intravenous steroids as per usual pediatric asthma management. |
| Evidence from published studies | Published studies and reviews suggest IV magnesium sulfate as an adjunct can benefit children with acute asthma, especially in severe cases. Its role in moderate exacerbations is still under investigation, with some evidence for reducing hospitalization rates in select patients. | Usual emergency asthma therapies are supported by robust evidence as effective first-line management for moderate asthma exacerbations in children. |
| Important limitations | While magnesium sulfate is generally safe when properly administered, the benefit in moderate asthma attacks is less clear than in severe cases. Risks include low blood pressure and flushing. More research is needed to define ideal timing and patient selection. | Standard asthma therapies are effective but some children may not respond adequately, which can lead to longer emergency department stays or need for additional therapies. |
Disclaimer: This comparison is created with the help of artificial intelligence(AI) and may contain errors or missing information. It is not medical advice and does not mean one option is better or safer than another. Clinical trials are still being studied, and joining a trial is your choice. Please consult your healthcare professional before making any decisions.
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 1 week
Participants receive either weight-based IV magnesium sulfate within the first hour alongside first line asthma therapies or standard care without early magnesium sulfate.
1 treatment visit during emergency department stay
Duration - Up to 2 weeks
Participants are monitored for need of respiratory support and clinical outcomes after treatment.
Continuous monitoring during hospital stay
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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Lead Sponsor