Nebulized Magnesium Sulfate as an Adjunct to Standard Therapy in Asthma Exacerbation
Primary Purpose
Asthma
Status
Unknown status
Phase
Phase 4
Locations
Mexico
Study Type
Interventional
Intervention
Nebulized Magnesium Sulfate
Nebulized isotonic saline
Nebulized Salbutamol
Ipratropium bromide
Methylprednisolone or Prednisolone
Sponsored by

About this trial
This is an interventional treatment trial for Asthma focused on measuring Asthma, Exacerbation, Nebulization, Magnesium, Pediatric
Eligibility Criteria
Inclusion Criteria:
- Clinical diagnosis of moderate or severe asthma exacerbations
- 2 to 15 years old.
- Served in the pediatric emergency department of naval high specialty General Hospital from September to December 2015.
- Signing the consent by the parents.
Exclusion Criteria:
- Coexistence of lung disease.
- Severe kidney disease.
- Severe liver disease.
- Pregnancy.
- Known previous reaction to magnesium.
- Parents who have not signed the agreement.
- Patients without a clinical history of asthma.
- Clinical diagnosis of mild asthma attack.
- Previously included in the study.
- Presence of comorbidities that endanger the patient's life.
- The patient has clinical or gasometric criteria for advanced airway management.
- Life-threatening symptoms.
Sites / Locations
- Hospital General Naval de Alta EspecialidadRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Nebulized Magnesium Sulfate
Nebulized isotonic saline
Arm Description
Nebulized salbutamol and ipratropium bromide mixed with 2.5 ml of isotonic MgSO4. Intravenous methylprednisolone or oral prednisolone
Nebulized salbutamol and ipratropium bromide with 2.5 ml of isotonic saline. Intravenous methylprednisolone or oral prednisolone
Outcomes
Primary Outcome Measures
Change from Baseline Preschool Respiratory Assessment Measure (PRAM)
Scalene muscle contraction, Suprasternal retractions, Wheezing, Air entry and O2 saturation.
The score will be considering from the addition per each primary measure.
Change from Baseline Scalene muscle contraction
Absent (0) or Present (2)
Change from Baseline Suprasternal retractions
Absent (0) or Present (2)
Change from Baseline Wheezing
Normal (0), Decreased at bases (1), Widespread decrease (2), or Absent/minimal (3)
Change from Baseline Air entry
Absent (0), Expiratory only (1), Inspiratory and expiratory (2) or Audible without (3) stethoscope/silent chest with minimal air entry
Change from Baseline O2 saturation
≥95% (0), 92%-94% (1) or <92% (2)
Secondary Outcome Measures
Rate of hospitalization
Reduction the rate of hospitalization
Change from Baseline Heart rate
Beats per minute
Change from Baseline Respiratory rate
Breaths per minute
Change from Baseline Blood pressure
mmHg
Full Information
NCT ID
NCT02584738
First Posted
October 14, 2015
Last Updated
November 30, 2015
Sponsor
Hospital General Naval de Alta Especialidad - Escuela Medico Naval
1. Study Identification
Unique Protocol Identification Number
NCT02584738
Brief Title
Nebulized Magnesium Sulfate as an Adjunct to Standard Therapy in Asthma Exacerbation
Official Title
Efficacy of Nebulized Magnesium Sulfate as an Adjunct to Standard Therapy in Asthma Exacerbation. A Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2015
Overall Recruitment Status
Unknown status
Study Start Date
September 2015 (undefined)
Primary Completion Date
January 2016 (Anticipated)
Study Completion Date
January 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital General Naval de Alta Especialidad - Escuela Medico Naval
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to investigate the effectiveness of nebulized magnesium sulfate in patient with moderate to severe asthma exacerbation in pediatric emergency
Detailed Description
The inclusion period of the patients in this research will be on September 2015 to November 2015. Patients are going to be selected by the medical staff on duty in the emergency paediatric service, according to the criteria previously established inclusion and exclusion. Immediately a baseline degree of respiratory distress using PRAM scale and heart rate, respiratory rate, blood pressure and oxygen saturation. While informed consent in which the objective and characteristics of the study will be obtained will be explained.
Patients will be randomly assigned one of the two treatments in the Research: standard treatment for moderate to severe asthma attack, according to GINA or standard treatment plus nebulised magnesium sulphate, according to the table of random allocation of treatment.
Evaluations were performed after administration of each spray, that is, at 20, 40, 60, 120, 180 and 240 minutes after beginning treatment. The parameters' to evaluate are going to be heart rate, respiratory rate, oxygen saturation, blood pressure and assessment of severity of acute asthma with PRAM scale.
The application of nebulized drugs are made in the emergency department of pediatrics by inhalation therapy staff who are also responsible for the preparation of medicines. It is clear that this staff not participate in the evaluation of patients, which will be performed by the research staff or by medical staff on duty in the pediatric emergency department.
Patients and evaluating physician will not pick out between the two solutions for nebulization not only colour but also smell or other special feature, because the solutions were arranged in two identical syringes. Administered alone at the end of the study treatment is known.
Later the entry or exit of the patient decide, who can be egress to show clinical improvement with decreased severity index PRAM, patients will be graduates of an outpatient treatment according to international guidelines on the management of acute asthma. All initial and outcome data will be recorded in a format of data collection All decisions will be made by patients pediatricians emergency department which will follow patients throughout the study and will have the power to release the study patients to use other interventions that they consider clinically necessary
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma
Keywords
Asthma, Exacerbation, Nebulization, Magnesium, Pediatric
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
152 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Nebulized Magnesium Sulfate
Arm Type
Experimental
Arm Description
Nebulized salbutamol and ipratropium bromide mixed with 2.5 ml of isotonic MgSO4.
Intravenous methylprednisolone or oral prednisolone
Arm Title
Nebulized isotonic saline
Arm Type
Placebo Comparator
Arm Description
Nebulized salbutamol and ipratropium bromide with 2.5 ml of isotonic saline. Intravenous methylprednisolone or oral prednisolone
Intervention Type
Drug
Intervention Name(s)
Nebulized Magnesium Sulfate
Other Intervention Name(s)
MgSO4
Intervention Description
Nebulized salbutamol and ipratropium bromide mixed with 2.5 ml of isotonic MgSO4 (150 mg) per dose every 20 minutes during the first hour.
will be continued with nebulized standard treatment every hour for 4 hours.
Intervention Type
Drug
Intervention Name(s)
Nebulized isotonic saline
Other Intervention Name(s)
Standard treatment
Intervention Description
Nebulized salbutamol and ipratropium bromide mixed with 2.5 ml of isotonic saline per dose every 20 minutes during the first hour.
will be continued with nebulized standard treatment every hour for 4 hours.
Intervention Type
Drug
Intervention Name(s)
Nebulized Salbutamol
Intervention Description
Nebulized salbutamol 2.5mg (2-5 years) or 5 mg (≥6 years)
Intervention Type
Drug
Intervention Name(s)
Ipratropium bromide
Intervention Description
Nebulized ipratropium bromide 250 mcg
Intervention Type
Drug
Intervention Name(s)
Methylprednisolone or Prednisolone
Other Intervention Name(s)
Corticosteroid therapy
Intervention Description
Begin with intravenous methylprednisolone or oral prednisolone 2 mg/kg/day for each treatment
Primary Outcome Measure Information:
Title
Change from Baseline Preschool Respiratory Assessment Measure (PRAM)
Description
Scalene muscle contraction, Suprasternal retractions, Wheezing, Air entry and O2 saturation.
The score will be considering from the addition per each primary measure.
Time Frame
20, 40, 60, 120, 180 and 240 minutes after beginning treatment
Title
Change from Baseline Scalene muscle contraction
Description
Absent (0) or Present (2)
Time Frame
20, 40, 60, 120, 180 and 240 minutes after beginning treatment
Title
Change from Baseline Suprasternal retractions
Description
Absent (0) or Present (2)
Time Frame
20, 40, 60, 120, 180 and 240 minutes after beginning treatment
Title
Change from Baseline Wheezing
Description
Normal (0), Decreased at bases (1), Widespread decrease (2), or Absent/minimal (3)
Time Frame
20, 40, 60, 120, 180 and 240 minutes after beginning treatment
Title
Change from Baseline Air entry
Description
Absent (0), Expiratory only (1), Inspiratory and expiratory (2) or Audible without (3) stethoscope/silent chest with minimal air entry
Time Frame
20, 40, 60, 120, 180 and 240 minutes after beginning treatment
Title
Change from Baseline O2 saturation
Description
≥95% (0), 92%-94% (1) or <92% (2)
Time Frame
20, 40, 60, 120, 180 and 240 minutes after beginning treatment
Secondary Outcome Measure Information:
Title
Rate of hospitalization
Description
Reduction the rate of hospitalization
Time Frame
4 hour
Title
Change from Baseline Heart rate
Description
Beats per minute
Time Frame
20, 40, 60, 120, 180 and 240 minutes after beginning treatment
Title
Change from Baseline Respiratory rate
Description
Breaths per minute
Time Frame
20, 40, 60, 120, 180 and 240 minutes after beginning treatment
Title
Change from Baseline Blood pressure
Description
mmHg
Time Frame
60 minutes after beginning treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Clinical diagnosis of moderate or severe asthma exacerbations
2 to 15 years old.
Served in the pediatric emergency department of naval high specialty General Hospital from September to December 2015.
Signing the consent by the parents.
Exclusion Criteria:
Coexistence of lung disease.
Severe kidney disease.
Severe liver disease.
Pregnancy.
Known previous reaction to magnesium.
Parents who have not signed the agreement.
Patients without a clinical history of asthma.
Clinical diagnosis of mild asthma attack.
Previously included in the study.
Presence of comorbidities that endanger the patient's life.
The patient has clinical or gasometric criteria for advanced airway management.
Life-threatening symptoms.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jesús Abisai Uicab Saucedo, Pediatrician
Phone
(52)5550371200
Ext
5423
Email
abisaipec@msn.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jesús Abisai Uicab Saucedo, Pediatrician
Organizational Affiliation
Secretaria de Marina
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital General Naval de Alta Especialidad
City
México
State/Province
Distrito Federal
ZIP/Postal Code
04480
Country
Mexico
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jesús Abisai Uicab Saucedo, Pediatrician
Phone
(52)5550371200
Ext
5423
Email
abisaipec@msn.com
12. IPD Sharing Statement
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Links:
URL
http://www.ginasthma.org
Description
Global Initiative for Asthma (GINA). Global strategy for asthma management and prevention (Updated 2015).
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Nebulized Magnesium Sulfate as an Adjunct to Standard Therapy in Asthma Exacerbation
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