Trials / Completed
CompletedNCT02145520
Efficacy of Magnesium Sulfate in the Treatment of Bronchiolitis
Efficacy of Magnesium Sulfate in the Treatment of Bronchiolitis.
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 200 (actual)
- Sponsor
- Hamad Medical Corporation · Industry
- Sex
- All
- Age
- 1 Month – 18 Months
- Healthy volunteers
- Accepted
Summary
In this study, investigators will compare the efficacy and safety of intravenous (IV) Magnesium sulfate in decreasing bronchiolitis clinical severity score and the duration of hospitalization in admitted patients, as compared to placebo.
Detailed description
* On arrival to Pediatric Emergency Center, patients will be attended by a pediatric specialist on call who will take history and perform full physical examination. Patients will be assessed for eligibility to the study based on the inclusion criteria. * Guardians of eligible patients will be approached with the study design, objectives and risks; Patients will be included after obtaining a verbal and assigned written consent. * A chest radiograph and Magnesium level in serum will be requested for all study patients upon recruitment. * The observation physician will complete the data collection sheet that will include the patient's demographics, physical examination, bronchiolitis clinical severity score,oxygen saturation, chest radiograph findings and Magnesium level. * Treatment will be delivered to enrolled patients as currently practice in PEC(Nebulized epinephrine 1:1000 1ml in 5 ml of 5% hypertonic saline, every 4 hours until discharge, for all patients and if there is history of Bronchial Asthma in mother, father or full sibling. And/or history of Eczema in the Child ,patients will start on dexamethasone 1mg/kg orally stat.(max-10 mg/dose). Then 0,6 mg/kg orally once daily starting from second day of admission for 4 days). * All patients will be randomized to receive either Magnesium sulfate intravenous single dose over 1 hour or placebo. And it will be given in the same time with currently practice treatment * Epinephrine nebulization can be given on PRN basis up to a maximum of every one hour, at a dose of 0.5 mg/kg (min 2.5mg/dose and max 5 mg/dose) mixed in 5 ml of 5% hypertonic saline.• * Bronchiolitis severity score (BSS) will be recorded at 0, 4, 8, 12, 16,20,24,36,48,60,72 hours, and on discharge. * Vital signs will be recorded at 0, 2, 4 hours and then every 4 hours from the administration of study medication. * All patients will be followed up for two weeks post discharge by a phone call asking about the general condition, relapse of symptoms, or need for readmission.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Magnesium Sulfate | The use of magnesium sulfate intravenous in patient with bronchiolitis in pediatric emergency; follow Broncholitis severity score and length of stay |
| OTHER | placebo | use of placebo with standard therapy |
Timeline
- Start date
- 2012-10-01
- Primary completion
- 2015-05-01
- Completion
- 2015-12-01
- First posted
- 2014-05-23
- Last updated
- 2016-08-16
Locations
1 site across 1 country: Qatar
Source: ClinicalTrials.gov record NCT02145520. Inclusion in this directory is not an endorsement.