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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02003911
Other study ID # 12-05-187
Secondary ID
Status Terminated
Phase Phase 4
First received
Last updated
Start date October 2013
Est. completion date June 1, 2018

Study information

Verified date August 2020
Source Montefiore Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Terminated
Enrollment 159
Est. completion date June 1, 2018
Est. primary completion date June 1, 2018
Accepts healthy volunteers No
Gender All
Age group 4 Years to 12 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Azithromycin
Azithromycin suspension (200mg/5mL)
Placebo


Locations

Country Name City State
United States The Children's Hospital at Montefiore Bronx New York

Sponsors (1)

Lead Sponsor Collaborator
Montefiore Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other 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. One week after discharge
Primary Length of Stay Hospital length of stay Admission time to discharge time (average LOS is 3 days)
Secondary 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
Secondary School Missed Days of school missed by patient at telephone follow-up phone calls at 1-week and 1-month interval after discharge 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 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 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 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 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 One month after discharge
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