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Low accrual
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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.
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Azithromycin suspension | Experimental | Azithromycin suspension at 10mg/kg/dose (max 500mg) Once daily for 3 days |
|
| Placebo suspension | Placebo Comparator | Same volume as active drug Once daily for 3 days |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Azithromycin | Drug | Azithromycin suspension (200mg/5mL) |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Length of Stay | Hospital length of stay | Admission time to discharge time (average LOS is 3 days) |
| Measure | Description | Time Frame |
|---|---|---|
| Readmission Rate | Number of hospital readmissions for asthma at telephone follow-up phone calls at 1-week and 1-month interval after discharge | One month 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 |
| Measure | Description | Time Frame |
|---|---|---|
| Routine Clinical Results and Symptoms | 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. |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Lindsey C Douglas, MD | Montefiore Medical Center | Principal Investigator |
| Katherine O'Connor, MD | Montefiore Medical Center | Study Director |
| Diana S. Lee, MD | Montefiore Medical Center | Study Director |
| Alyssa H Silver, MD | Montefiore Medical Center | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The Children's Hospital at Montefiore | The Bronx | New York | 10467 | United States |
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| ID | Title | Description |
|---|---|---|
| FG000 | Azithromycin Suspension | Azithromycin suspension at 10mg/kg/dose (max 500mg) Once daily for 3 days Azithromycin: Azithromycin suspension (200mg/5mL) |
| FG001 | Placebo Suspension | Same volume as active drug Once daily for 3 days Placebo |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Azithromycin Suspension | Azithromycin suspension at 10mg/kg/dose (max 500mg) Once daily for 3 days Azithromycin: Azithromycin suspension (200mg/5mL) |
| BG001 | Placebo Suspension |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Median |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Length of Stay | Hospital length of stay | Posted | Median | Inter-Quartile Range | days | Admission time to discharge time (average LOS is 3 days) |
|
|
One month
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Azithromycin Suspension | Azithromycin suspension at 10mg/kg/dose (max 500mg) Once daily for 3 days Azithromycin: Azithromycin suspension (200mg/5mL) |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Transfer to PICU | Respiratory, thoracic and mediastinal disorders | Non-systematic Assessment |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Study Exit | Social circumstances | Non-systematic Assessment |
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Dr. Lindsey Douglas | Mount Sinai Kravis Children's Hospital | 2122416500 | lindsey.douglas@mssm.edu |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Dec 4, 2013 | Feb 25, 2020 | Prot_SAP_000.pdf |
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| ID | Term |
|---|---|
| D001249 | Asthma |
| ID | Term |
|---|---|
| D001982 | Bronchial Diseases |
| D012140 | Respiratory Tract Diseases |
| D008173 | Lung Diseases, Obstructive |
| D008171 | Lung Diseases |
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| ID | Term |
|---|---|
| D017963 | Azithromycin |
| ID | Term |
|---|---|
| D004917 | Erythromycin |
| D018942 | Macrolides |
| D061065 | Polyketides |
| D007783 | Lactones |
| D009930 |
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| Placebo |
| Drug |
|
| One month 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 | One month 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 | One month 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 | One month 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 | One month after discharge |
| Steroid Courses | Number of courses of oral steroids since discharge at telephone follow-up phone call 1-month after discharge | One month after discharge |
| One week after discharge |
Same volume as active drug
Once daily for 3 days
Placebo
| BG002 | Total | Total of all reporting groups |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
|
| Race (NIH/OMB) | Count of Participants | Participants |
|
| PASS Score on enrollment | PASS=Pediatric Asthma Severity Score Range 0 (best) - 6 (worst) Score at each time point is calculated by adding 3 elements: Wheeze (0= None/Mild, 1=Moderate, 2=Severe) Prolonged expiration (0= None/Mild, 1=Moderate, 2=Severe) Work of breathing (0= None/Mild, 1=Moderate, 2=Severe) | Mean | Standard Deviation | Score on a scale |
|
| Participants |
|
|
| Secondary | Readmission Rate | Number of hospital readmissions for asthma at telephone follow-up phone calls at 1-week and 1-month interval after discharge | Posted | Count of Participants | Participants | One month after discharge |
|
|
|
| Secondary | School Missed | Days of school missed by patient at telephone follow-up phone calls at 1-week and 1-month interval after discharge | Posted | Count of Participants | Participants | One month after discharge |
|
|
|
| Secondary | Work Missed | Days of work missed by parent/guardian at telephone follow-up phone calls at 1-week and 1-month interval after discharge | Posted | Count of Participants | Participants | One month after discharge |
|
|
|
| Secondary | 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 | Posted | Count of Participants | Participants | One month after discharge |
|
|
|
| Secondary | 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 | Posted | Count of Participants | Participants | One month after discharge |
|
|
|
| Secondary | 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 | Posted | Count of Participants | Participants | One month after discharge |
|
|
|
| Secondary | Steroid Courses | Number of courses of oral steroids since discharge at telephone follow-up phone call 1-month after discharge | Posted | Count of Participants | Participants | One month after discharge |
|
|
|
| Other Pre-specified | Routine Clinical Results and Symptoms | 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. | Not Posted | One week after discharge | Participants |
| 0 |
| 80 |
| 0 |
| 80 |
| 2 |
| 80 |
| EG001 | Placebo Suspension | Same volume as active drug Once daily for 3 days Placebo | 0 | 79 | 1 | 79 | 7 | 79 |
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| D012130 |
| Respiratory Hypersensitivity |
| D006969 | Hypersensitivity, Immediate |
| D006967 | Hypersensitivity |
| D007154 | Immune System Diseases |
| Organic Chemicals |