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Azithromycin for Children Hospitalized With Asthma

A Double-Blind, Randomized, Placebo-Controlled Trial of Azithromycin in Children Hospitalized With Acute Asthma Exacerbations

Status
Terminated
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02003911
Enrollment
159
Registered
2013-12-06
Start date
2013-10-31
Completion date
2018-06-01
Last updated
2020-08-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma

Keywords

Asthma, Acute asthma exacerbation, Pediatric, Azithromycin, Macrolide, Length of Stay, Hospital Medicine

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.

Interventions

DRUGAzithromycin

Azithromycin suspension (200mg/5mL)

DRUGPlacebo

Sponsors

Montefiore Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
4 Years to 12 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Length of StayAdmission time to discharge time (average LOS is 3 days)Hospital length of stay

Secondary

MeasureTime frameDescription
School MissedOne month after dischargeDays of school missed by patient at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Readmission RateOne month after dischargeNumber of hospital readmissions for asthma at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Work MissedOne month after dischargeDays of work missed by parent/guardian at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Physician Office VisitsOne month after dischargeNumber 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 SymptomsOne month after dischargeNumber of recurrences of asthma symptoms since discharge at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Steroid CoursesOne month after dischargeNumber of courses of oral steroids since discharge at telephone follow-up phone call 1-month after discharge
Emergency Room VisitsOne month after dischargeNumber of emergency room visits for asthma symptoms since discharge at telephone follow-up phone calls at 1-week and 1-month interval after discharge

Other

MeasureTime frameDescription
Routine Clinical Results and SymptomsOne week after dischargeRespiratory 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.

Countries

United States

Participant flow

Participants by arm

ArmCount
Azithromycin Suspension
Azithromycin suspension at 10mg/kg/dose (max 500mg) Once daily for 3 days Azithromycin: Azithromycin suspension (200mg/5mL)
80
Placebo Suspension
Same volume as active drug Once daily for 3 days Placebo
79
Total159

Baseline characteristics

CharacteristicAzithromycin SuspensionPlacebo SuspensionTotal
Age, Continuous7.5 years7.1 years7.3 years
Ethnicity (NIH/OMB)
Hispanic or Latino
55 Participants56 Participants111 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
25 Participants23 Participants48 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
PASS Score on enrollment2.35 Score on a scale
STANDARD_DEVIATION 1.25
2.71 Score on a scale
STANDARD_DEVIATION 1.29
2.53 Score on a scale
STANDARD_DEVIATION 1.28
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
40 Participants33 Participants73 Participants
Race (NIH/OMB)
More than one race
29 Participants32 Participants61 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
11 Participants14 Participants25 Participants
Sex: Female, Male
Female
29 Participants26 Participants55 Participants
Sex: Female, Male
Male
51 Participants53 Participants104 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 800 / 79
other
Total, other adverse events
2 / 807 / 79
serious
Total, serious adverse events
0 / 801 / 79

Outcome results

Primary

Length of Stay

Hospital length of stay

Time frame: Admission time to discharge time (average LOS is 3 days)

ArmMeasureValue (MEDIAN)
Azithromycin SuspensionLength of Stay1.69 days
Placebo SuspensionLength of Stay1.86 days
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

Time frame: One month after discharge

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Azithromycin SuspensionEmergency Room Visits6 Participants
Placebo SuspensionEmergency Room Visits7 Participants
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

Time frame: One month after discharge

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Azithromycin SuspensionPhysician Office Visits7 Participants
Placebo SuspensionPhysician Office Visits5 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

Time frame: One month after discharge

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Azithromycin SuspensionReadmission Rate1 Participants
Placebo SuspensionReadmission Rate1 Participants
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

Time frame: One month after discharge

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Azithromycin SuspensionRecurrence of Asthma Symptoms18 Participants
Placebo SuspensionRecurrence of Asthma Symptoms23 Participants
Secondary

School Missed

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

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Azithromycin SuspensionSchool Missed0 Participants
Placebo SuspensionSchool Missed0 Participants
Secondary

Steroid Courses

Number of courses of oral steroids since discharge at telephone follow-up phone call 1-month after discharge

Time frame: One month after discharge

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Azithromycin SuspensionSteroid Courses8 Participants
Placebo SuspensionSteroid Courses11 Participants
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

Time frame: One month after discharge

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Azithromycin SuspensionWork Missed0 Participants
Placebo SuspensionWork Missed0 Participants
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.

Time frame: One week after discharge

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026