Evaluation Montelukast in the Treatment of Status Asthmaticus
Primary Purpose
Status Asthmaticus
Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Montelukast
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Status Asthmaticus focused on measuring Montelukast, Singulair, status asthmaticus
Eligibility Criteria
Inclusion criteria:
- Between ages 2-148 years
- Requiring PICU admission for status asthmaticus
- Able to take oral medication
- Pediatric asthma score > 8 on admission
Exclusion criteria:
- Intubated patients or other patients unable to take medications by mouth secondary to anatomic or pre-existing craniofacial issues
- Patients already on montelukast as their controller medication
- Patients with a known allergy to montelukast
- Any patient with phenylketonuria (PKU)
- Any patient currently on treatment with rifampin, fluconazole, or Phenobarbital medications
Sites / Locations
- Advocate Children's Hospital Oak LawnRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Montelukast
Placebo
Arm Description
Montelukast 5mg capsules for 2-5 year old every 24h and 8mg capsules for 6-14 year olds every 24h.
One placebo capsule given every 24h
Outcomes
Primary Outcome Measures
Improvement of pediatric asthma score
Measurement of pediatric asthma score hourly from admission assessing for time to improvement of score, an average length of stay predicted 2-4 days.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01770899
Brief Title
Evaluation Montelukast in the Treatment of Status Asthmaticus
Official Title
A Prospective Analysis of the Use of Oral Montelukast in Children With Status Asthmaticus
Study Type
Interventional
2. Study Status
Record Verification Date
February 2013
Overall Recruitment Status
Unknown status
Study Start Date
January 2013 (undefined)
Primary Completion Date
December 2013 (Anticipated)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Corrie Fletcher
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to evaluate the effectiveness of oral montelukast (Singulair) given with other standard asthma medications and treatments in the treatment of children with status asthmaticus. Status asthmaticus is an acute asthma attack that does not respond to standard intermittent treatments but requires a continuous medication to aid in breathing. While new medications have been used to better manage chronic asthma, acute asthma exacerbations continue to be a significant cause of hospitalization and even death in children. Oral montelukast is a very safe medication that is used to manage chronic asthma in children, but it has not been studied for use in status asthmaticus. If oral montelukast, given with other standard therapies, can reduce the treatment length associated with severe, acute asthma exacerbations in children, it could potentially improve both the morbidity and burden of pediatric asthma.
Detailed Description
While new medications have been used to better manage chronic asthma, acute exacerbations continue to be a significant cause of pediatric morbidity and mortality. Montelukast holds an established role in the pediatric outpatient management of asthma and while two promising studies in adults have demonstrated its potential use as an adjunctive therapy for acute exacerbations, its similar use in pediatrics has yet to be established. This pilot study is designed as a prospective, double blinded, randomized, controlled, clinical trial comparing the use of oral montelukast plus standard of care vs. standard of care alone in children admitted for status asthmaticus to the pediatric intensive care unit (PICU). The primary outcome the investigators are interested in is the time to reach a Modified Pediatric Asthma Score (PAS) of < 5, which, per the clinical protocol for the treatment of status asthmaticus, is the time when patients are able to come off continuous bronchodilator therapy. If oral montelukast, given with other standard therapies, can reduce the treatment, emotional, and financial burden (e.g., shortened intensive care stay) associated with severe, acute asthma exacerbations in children, it would provide a significant therapeutic advantage, potentially improving both the morbidity and burden of pediatric asthma.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Status Asthmaticus
Keywords
Montelukast, Singulair, status asthmaticus
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Montelukast
Arm Type
Experimental
Arm Description
Montelukast 5mg capsules for 2-5 year old every 24h and 8mg capsules for 6-14 year olds every 24h.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
One placebo capsule given every 24h
Intervention Type
Drug
Intervention Name(s)
Montelukast
Other Intervention Name(s)
Singulair
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Gelatin capsule given every 24 hours
Primary Outcome Measure Information:
Title
Improvement of pediatric asthma score
Description
Measurement of pediatric asthma score hourly from admission assessing for time to improvement of score, an average length of stay predicted 2-4 days.
Time Frame
Hourly during the length of the patient's pediatric ICU hospitalization for status asthmaticus
10. Eligibility
Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria:
Between ages 2-148 years
Requiring PICU admission for status asthmaticus
Able to take oral medication
Pediatric asthma score > 8 on admission
Exclusion criteria:
Intubated patients or other patients unable to take medications by mouth secondary to anatomic or pre-existing craniofacial issues
Patients already on montelukast as their controller medication
Patients with a known allergy to montelukast
Any patient with phenylketonuria (PKU)
Any patient currently on treatment with rifampin, fluconazole, or Phenobarbital medications
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Corrie E Fletcher, DO
Phone
708-684-1308
Email
corrie.fletcher@advocatehealth.com
First Name & Middle Initial & Last Name or Official Title & Degree
Luis Torero, MD
Phone
708-684-5685
Email
luis.torero@advocatehealth.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Corrie Fletcher, DO
Organizational Affiliation
Advocate Health Care
Official's Role
Principal Investigator
Facility Information:
Facility Name
Advocate Children's Hospital Oak Lawn
City
Oak Lawn
State/Province
Illinois
ZIP/Postal Code
60453
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Corrie Fletcher, DO
12. IPD Sharing Statement
Learn more about this trial
Evaluation Montelukast in the Treatment of Status Asthmaticus
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