Azithromycin for Children Hospitalized With Asthma
Primary Purpose
Asthma
Status
Terminated
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Azithromycin
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Asthma focused on measuring Asthma, Acute asthma exacerbation, Pediatric, Azithromycin, Macrolide, Length of Stay, Hospital Medicine
Eligibility Criteria
Inclusion Criteria:
- 4-12 years of age
- Admission diagnosis of asthma at the Children's Hospital at Montefiore
- History of persistent asthma (as defined by National Heart, Lung, and Blood Institute)
Exclusion Criteria:
- Concurrent bacterial infection requiring antibiotics
- Antibiotics received within previous 2 weeks
- Contraindication to azithromycin (including allergy to macrolides)
- Chronic lung disease other than asthma (including bronchopulmonary dysplasia, cystic fibrosis, bronchiectasis) or home oxygen requirement
- Immunodeficiency (primary or acquired)
- Chronic systemic steroid use
- Invasive or non-invasive mechanical ventilation required acutely as result of current asthma admission
- Significant cardiac co-morbidity (including hemodynamically significant cardiac disease or arrhythmia)
- Liver disease (hepatitis)
- Pregnancy
- Seizure disorder, currently on anti-epileptic medication)
- Receiving albuterol every 4 hours (q4h) at the time of enrollment
- Previous enrollment in study
Sites / Locations
- The Children's Hospital at Montefiore
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Azithromycin suspension
Placebo suspension
Arm Description
Azithromycin suspension at 10mg/kg/dose (max 500mg) Once daily for 3 days
Same volume as active drug Once daily for 3 days
Outcomes
Primary Outcome Measures
Length of Stay
Hospital length of stay
Secondary Outcome Measures
Readmission Rate
Number of hospital readmissions for asthma at telephone follow-up phone calls at 1-week and 1-month interval after discharge
School Missed
Days of school missed by patient at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Work Missed
Days of work missed by parent/guardian at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Emergency Room Visits
Number of emergency room visits for asthma symptoms since discharge at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Physician Office Visits
Number of physician office visits for asthma symptoms since discharge at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Recurrence of Asthma Symptoms
Number of recurrences of asthma symptoms since discharge at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Steroid Courses
Number of courses of oral steroids since discharge at telephone follow-up phone call 1-month after discharge
Full Information
NCT ID
NCT02003911
First Posted
November 21, 2013
Last Updated
August 11, 2020
Sponsor
Montefiore Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT02003911
Brief Title
Azithromycin for Children Hospitalized With Asthma
Official Title
A Double-Blind, Randomized, Placebo-Controlled Trial of Azithromycin in Children Hospitalized With Acute Asthma Exacerbations
Study Type
Interventional
2. Study Status
Record Verification Date
August 2020
Overall Recruitment Status
Terminated
Why Stopped
Low accrual
Study Start Date
October 2013 (Actual)
Primary Completion Date
June 1, 2018 (Actual)
Study Completion Date
June 1, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Montefiore Medical Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Asthma is a chronic lung condition in children, and often requires hospitalization for acute exacerbations. Azithromycin has been used successfully in other chronic lung diseases, including cystic fibrosis. Despite limited clinical evidence, some pediatricians use azithromycin in children hospitalized with asthma, citing either treatment of atypical pathogens or its proposed anti-inflammatory properties. This study proposes a clinical trial to determine if azithromycin will shorten length of stay in children hospitalized with acute asthma exacerbations.
Detailed Description
Asthma is a chronic lung condition that accounts for over 130,000 pediatric hospitalizations nationally at a cost of almost 1.4 billion dollars. Atypical pathogens have been implicated both in initiating asthma and triggering acute asthma exacerbations. Azithromycin, a macrolide antibiotic, is known to have antibacterial activity against atypical pathogens and gram positive bacteria. More recently, macrolides have been increasingly used and effective against gram negative bacteria and inflammation in the lungs of patients with chronic respiratory illnesses. This effect may be secondary to the immunomodulatory effects macrolides possess, in addition to their anti-bacterial effects. In long-term therapy with macrolides, patients with asthma have shown improved bronchiolar hyperreactivity, spirometry, symptoms, and quality of life. However, studies of short-term treatment in the acute setting and in children are limited. Some practitioners use azithromycin in the treatment of acute asthma, despite limited data.
The investigators propose a double-blind, randomized, placebo-controlled trial of azithromycin in children aged 4-12 years with persistent asthma hospitalized with acute asthma exacerbations. Children will be enrolled within 12 hours of admission and will be randomized to receive three days of either azithromycin or placebo suspension (10mg/kg/dose, max of 500mg). The primary outcome measure will be length of stay (LOS). Secondary outcome measures will include: days of school/work missed, readmission rates, return to medical care rates, recurrence of symptoms, and steroid courses. In the future, patients may also be approached to enroll in the "Mechanism Subset Study" a separate pilot and feasibility study which will require two blood samples and two nasal aspirate samples and will test for atypical pathogens, interleukin-8 levels, and neutrophil/eosinophil counts. The average length of stay for patients in this age range with asthma in 2011 at our institution was 3.0 days. The investigators will enroll to achieve a power of 80%, with an alpha of 0.05, which will require 107 patients in each group to detect a 16 hour (0.67 day) difference in the primary outcome, LOS. This study hypothesizes that azithromycin treatment in children hospitalized with acute asthma will decrease LOS.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma
Keywords
Asthma, Acute asthma exacerbation, Pediatric, Azithromycin, Macrolide, Length of Stay, Hospital Medicine
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
159 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Azithromycin suspension
Arm Type
Experimental
Arm Description
Azithromycin suspension at 10mg/kg/dose (max 500mg)
Once daily for 3 days
Arm Title
Placebo suspension
Arm Type
Placebo Comparator
Arm Description
Same volume as active drug
Once daily for 3 days
Intervention Type
Drug
Intervention Name(s)
Azithromycin
Intervention Description
Azithromycin suspension (200mg/5mL)
Intervention Type
Drug
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
Length of Stay
Description
Hospital length of stay
Time Frame
Admission time to discharge time (average LOS is 3 days)
Secondary Outcome Measure Information:
Title
Readmission Rate
Description
Number of hospital readmissions for asthma at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Time Frame
One month after discharge
Title
School Missed
Description
Days of school missed by patient at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Time Frame
One month after discharge
Title
Work Missed
Description
Days of work missed by parent/guardian at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Time Frame
One month after discharge
Title
Emergency Room Visits
Description
Number of emergency room visits for asthma symptoms since discharge at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Time Frame
One month after discharge
Title
Physician Office Visits
Description
Number of physician office visits for asthma symptoms since discharge at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Time Frame
One month after discharge
Title
Recurrence of Asthma Symptoms
Description
Number of recurrences of asthma symptoms since discharge at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Time Frame
One month after discharge
Title
Steroid Courses
Description
Number of courses of oral steroids since discharge at telephone follow-up phone call 1-month after discharge
Time Frame
One month after discharge
Other Pre-specified Outcome Measures:
Title
Routine Clinical Results and Symptoms
Description
Respiratory viral panel or rapid viral testing results (if obtained as part of medical care), chest x-ray results/lab results (if obtained as part of medical care), vital signs, medications received during admission, medication side effects (diarrhea, abdominal pain, vomiting, flatulence), transfer to intensive care unit, time of wean of beta-agonists (q3h and q4h), and asthma severity (PASS score) at time of enrollment.
Time Frame
One week after discharge
10. Eligibility
Sex
All
Minimum Age & Unit of Time
4 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
4-12 years of age
Admission diagnosis of asthma at the Children's Hospital at Montefiore
History of persistent asthma (as defined by National Heart, Lung, and Blood Institute)
Exclusion Criteria:
Concurrent bacterial infection requiring antibiotics
Antibiotics received within previous 2 weeks
Contraindication to azithromycin (including allergy to macrolides)
Chronic lung disease other than asthma (including bronchopulmonary dysplasia, cystic fibrosis, bronchiectasis) or home oxygen requirement
Immunodeficiency (primary or acquired)
Chronic systemic steroid use
Invasive or non-invasive mechanical ventilation required acutely as result of current asthma admission
Significant cardiac co-morbidity (including hemodynamically significant cardiac disease or arrhythmia)
Liver disease (hepatitis)
Pregnancy
Seizure disorder, currently on anti-epileptic medication)
Receiving albuterol every 4 hours (q4h) at the time of enrollment
Previous enrollment in study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lindsey C Douglas, MD
Organizational Affiliation
Montefiore Medical Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Katherine O'Connor, MD
Organizational Affiliation
Montefiore Medical Center
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Diana S. Lee, MD
Organizational Affiliation
Montefiore Medical Center
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Alyssa H Silver, MD
Organizational Affiliation
Montefiore Medical Center
Official's Role
Study Director
Facility Information:
Facility Name
The Children's Hospital at Montefiore
City
Bronx
State/Province
New York
ZIP/Postal Code
10467
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
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Azithromycin for Children Hospitalized With Asthma
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