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Comparasion of Efficacy of Nebulized With Intravenous Magnesium Sulphate in Children With Asthma

Phase 4
Completed
Conditions
Asthma in Children
Interventions
Drug: Nebulized Magnesium sulfate
Drug: Intravenous magnesium sulphate
Registration Number
NCT04497766
Lead Sponsor
Saima Khatoon
Brief Summary

The purpose of study is to assess the effectiveness of nebulized magnesium sulphate in children presenting with acute asthma.Study perfoma consists of demographic variables,exclusion criteria and pediatric asthma score that includes respiratory rate,SPO2 at room air(requirement of oxygen),auscultatory findings in chest,dysnea and retractions.

Detailed Description

After getting informed consent from guardian,148 patients of acute moderate ro severe asthma with pediatric asthma score 8-15 will be randomly classified into 2 groups and one group will receive nebulization with magnesium sulphate and other will receive intravenous magnesium sulphate and effectiveness will be compared by 4 point reduction in PAS from baseline in either groups after 6 hours.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
148
Inclusion Criteria
  • patients with age 2 to 12 years with acute moderate to severe exacerbation of asthma as per operational definition children who are unrespoinsive to standard treatment of asthma at 60 minutes
Exclusion Criteria
  • those with history of chronic lung disease and abnormal renal function contraindication for MgSO4 due to hepatic or renal disease allergy to MgSo4 children who has other comorbid illness

Study & Design

Study Type
INTERVENTIONAL
Study Design
FACTORIAL
Arm && Interventions
GroupInterventionDescription
Nebulized magnesium sulphateNebulized Magnesium sulfate100mg of mgso4 in 20ml of normal saline via ultrasonic nebulizer
Intravenous magnesium sulphateIntravenous magnesium sulphateMagnesium sulphate according to weight will be given intravenously.
Primary Outcome Measures
NameTimeMethod
Efficacy of nebulized magnesium sulphate with intravenous magnesium sulphate in children with acute asthma will be assessed by a drop in PAS score, as assessed at 6 hours of intervention.6 hours

The intervention will be considered effective if there is a drop of at least 4 points in PAS score at hour-6 of intervention.

Secondary Outcome Measures
NameTimeMethod
duration of hospital stay120 hours/5 days

this will be measured in hours

duration of ICU stay72 hours/3 days

this will be measured in hours

Trial Locations

Locations (1)

King edward medical university/mayo hospital lahore

🇵🇰

Lahore, Punjab, Pakistan

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