Use of Montelukast to Treat Children With Mild to Moderate Acute Asthma | RxWiki

Use of Montelukast to Treat Children With Mild to Moderate Acute Asthma

Overview[ - collapse ][ - ]

Purpose	The primary objective of this study is to evaluate if children with acute asthma given a single dose of oral prednisolone with a subsequent daily five-day course of oral Montelukast will achieve a therapeutic failure rate at day 8 not significantly higher than those given six daily doses of oral prednisolone. Secondary objectives include comparison of the two groups with respect to the changes in symptoms, beta2 agonists, clinical asthma score and days without asthma by day 8.
Condition	Asthma, Bronchial
Intervention	Drug: Montelukast plus prednisolone Drug: Prednisolone
Phase	Phase 2
Sponsor	The Hospital for Sick Children
Responsible Party	The Hospital for Sick Children
ClinicalTrials.gov Identifier	NCT00213252
First Received	September 13, 2005
Last Updated	March 11, 2010
Last verified	September 2006

Tracking Information[ + expand ][ + ]

First Received Date	September 13, 2005
Last Updated Date	March 11, 2010
Start Date	September 2005
Estimated Primary Completion Date	Not Provided
Current Primary Outcome Measures	Therapeutic failure rate [Time Frame: From randomization at discharge from the Emergency Department to day 8] [Designated as safety issue: No]
Current Secondary Outcome Measures	Number of inhaled salbutamol treatments [Time Frame: From randomization to 24, 48, 72, 96, 120, 144 hours and day 8] [Designated as safety issue: No] Change in the daytime asthma symptom scale from randomization [Time Frame: 48 hours and Day 8] [Designated as safety issue: No] Change in the nighttime cough [Time Frame: 8 days] [Designated as safety issue: No] Number of days without asthma [Time Frame: 8 days] [Designated as safety issue: No] Change in the Pulmonary Index Score from baseline [Time Frame: 48 hours and Day 8] [Designated as safety issue: No] Change in the Pediatric Respiratory Assessment Measure(PRAM)from baseline [Time Frame: 48 hours and Day 8] [Designated as safety issue: No] Association between the main treatment effect and patients' age, disease severity at randomization (Pulmonary Index and PRAM) and personal/family history of atopy. [Time Frame: 48 hours and Day 8] [Designated as safety issue: No]

Descriptive Information[ + expand ][ + ]

Brief Title	Use of Montelukast to Treat Children With Mild to Moderate Acute Asthma
Official Title	Can Montelukast Shorten Corticosteroid Therapy In Children With Mild To Moderate Acute Asthma?
Brief Summary	The primary objective of this study is to evaluate if children with acute asthma given a single dose of oral prednisolone with a subsequent daily five-day course of oral Montelukast will achieve a therapeutic failure rate at day 8 not significantly higher than those given six daily doses of oral prednisolone. Secondary objectives include comparison of the two groups with respect to the changes in symptoms, beta2 agonists, clinical asthma score and days without asthma by day 8.
Detailed Description	We plan a randomized double blind double-dummy trial of 190 previously healthy children 2-17 years of age presenting to the Emergency Department (ED) at the Hospital for Sick Children in Toronto with mild to moderate acute asthma, with the Pulmonary Index score ≤ 11 points and PRAM ≤ 8 points. Asthma will be defined as at least the second episode of wheezing, with signs of lower airway obstruction. All participating children will receive a single dose of oral prednisolone 2mg/kg (max 60 mg) on arrival and standardized inhaled salbutamol in the ED and for five days thereafter. At discharge from ED children will be randomized to two interventional groups. Those in the Montelukast group will get oral Montelukast 4 mg (2-5 year olds), 5 mg (6-14 year olds), and 10 mg (15-17 year olds) as well as daily prednis(ol)one placebo 24 hours after the ED dose of prednisolone and at 48, 72, 96 and 120 hours, while those in the prednisolone group will receive Montelukast placebo and daily oral prednisolone 1mg/kg (max 60 mg) for five further doses at these times. The primary outcome will be therapeutic failure in the two groups from randomization to day 8. This failure will be defined as unscheduled medical visits for asthma symptoms or hospitalization or treatment with oral corticosteroids outside the experimental protocol. Secondary outcome measures include comparison of the number of salbutamol treatments, changes in the previously validated daytime symptoms scale, nighttime cough/awakening scale, number of asthma-free days within the 8 day observational period in the two groups, changes in the PI and PRAM scores to 48 hours and day 8 as well as the association between the main treatment effect and age, pulmonary index at randomization and history of atopy. This study will take two 9 months periods. Primary analysis will include a one-sided 95% CI for the difference in failure rate in the prednisolone group minus the Montelukast group. Secondary analyses will include repeated measures ANOVA for differences in changes of continuous variables and the Fisher's Exact test for comparison of proportions. An exploratory sub-group logistic regression analysis will be done for examining interaction between the main treatment effect and possible covariates. In the event that the patients given a single dose of prednisolone followed by Montelukast have comparable therapeutic failure rate to those given standard extended prednisolone therapy, administration of Montelukast may help us abbreviate the length of corticosteroid therapy in children with acute asthma.
Study Type	Interventional
Study Phase	Phase 2
Study Design	Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
Condition	Asthma, Bronchial
Intervention	Drug: Montelukast plus prednisolone Single dose of oral prednisolone with a subsequent daily five-day course of oral Montelukast Drug: Prednisolone Six daily doses of oral prednisolone
Study Arm (s)	Experimental: 1 Active Comparator: 2

Recruitment Information[ + expand ][ + ]

Recruitment Status	Recruiting
Estimated Enrollment	190
Estimated Completion Date	Not Provided
Estimated Primary Completion Date	Not Provided
Eligibility Criteria	Inclusion Criteria: - age 2-17 years - Clinical diagnosis of mild to moderate asthma as a second wheezing episode associated with signs of respiratory distress suggesting lower airway obstruction such as tachypnea and/or use of accessory muscles of respiration. - baseline Pulmonary Index Clinical Score (Appendix B) ≤ 11 out of 15 possible points as well as PRAM ≤ 8 out of 12 points. - Presenting to the Sick Kids Emergency Department - Children capable of FEV1 measurement will have FEV1 more than 60% of the predicted value - male or female - Willing and able to provide informed consent (or informed consent by parents) Exclusion Criteria: - No previous history of wheezing or bronchodilator therapy. This population may eventually have diagnoses other than asthma or viral induced wheezing - Patients who received more than a single dose of oral corticosteroids within 72 hours prior to arrival - Patients receiving more than 500 mcg per day of fluticasone for more than 1 month or more than 250 mcg of fluticasone for more than 7 days prior to arrival - Patients who have had more than 2 previous visits to the asthma clinic at SickKids - Patients who received Montelukast within one week of arrival - Critically ill patients requiring airway stabilization - Patients with severe asthma, defined as PI 12 to 15 or PRAM 9 to 12. - Co-existent co-morbidities such as chronic pulmonary disease and cardiac disease requiring pharmacotherapy, neurologic disease and immune disorders. - Previous admission to ICU for asthma. - More than 3 hospitalizations for asthma during the past 12 months. - Contact with varicella within the previous 21 days. - Insufficient command of the English language
Gender	Both
Ages	2 Years
Accepts Healthy Volunteers	No
Contacts	Contact: Suzanne Schuh, MD 416-813-6239 suzanne.schuh@sickkids.ca
Location Countries	Canada

Administrative Information[ + expand ][ + ]

NCT Number	NCT00213252
Other Study ID Numbers	1000007674
Has Data Monitoring Committee	Yes
Information Provided By	The Hospital for Sick Children
Study Sponsor	The Hospital for Sick Children
Collaborators	Merck Frosst Canada Ltd.
Investigators	Principal Investigator: Suzanne Schuh, MD The Hospital for Sick Children, Toronto, Canada
Verification Date	September 2006

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