AZMATICS: AZithroMycin/Asthma Trial In Community Settings

Completed · Phase 3 · Has a placebo group

Conditions studied: Asthma

In brief

The purpose of this study is to assess the effectiveness of the azalide macrolide azithromycin in adults with persistent asthma. Research Question: Will a 12-week treatment with the antibiotic, azithromycin, result in a statistically significant and clinically meaningful improvement in overall asthma symptoms and other patient-oriented asthma outcomes one year after initiation of treatment of adult primary care patients with asthma? Experimental Design: The investigators propose a one-year randomized, placebo-controlled, blinded (investigator, patient, data collector, data analyst) trial of 12 weekly doses of azithromycin/placebo as adjunctive therapy (in addition to usual care) along with a parallel observational cohort who will participate 'open label' in 100 adult asthma patients recruited from practice-based research networks (e.g., Wisconsin Research and Education Network (WREN) and others). This "practical clinical trial" will (1) enroll a representative sample of asthma patients encountered in the practices of primary care physicians, (2) employ standard clinical trial methodology to ensure internally valid results and (3) measure outcomes important to patients, so that the results will be valid and applicable to the kinds of asthma patients encountered by family physicians and other primary care providers. Active study sites - * Wisconsin: Augusta, Cross Plains, La Crosse, Marshfield, Milwaukee, Madison, * Mauston, Rice Lake, Tomah, Wausau * Colorado: Monument * Illinois: Peoria * Nevada: Reno * North Carolina: Granite Falls * North Dakota: Minot * Ohio: Cleveland, Berea * Oklahoma: Ardmore, Claremore, Edmond, Lawton, Oklahoma City, Stroud, Tulsa, Weatherford * Rhode Island: East Providence

Key facts

Study ID: NCT00266851
Run by: University of Wisconsin, Madison
People needed: 97
Starts: 2006-01-01
Expected to finish: 2010-11-01
Last updated by the study team: 2019-09-06

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

Age 18 and older (and at least 50 kg/110 pounds)
The lower weight limit was chosen to avoid exposure to greater than 12 mg/kg/day of azithromycin (a currently recommended dose for children)
We specify no upper age limit because asthma occurs throughout the age range and because asthma in the elderly is particularly severe and warrants inclusion.
Physician-diagnosed asthma
At the time of randomization, eligible subjects must either:
be having a documented asthma exacerbation OR
be reporting at least mild persistent asthma symptoms, as defined by GINA (Global Initiative for Asthma)
Subjects must also have asthma symptoms for at least six months prior to randomization
Documentation of objective evidence of reversible airway obstruction, either spontaneously or after treatment, is required prior to randomization. This requirement can be met by documentary evidence, within 2 years of randomization, of either:
a 12% or greater (and ≥200 mL) change in FEV1 OR
a 25% or greater (and >60 L/min) change in PEFR either spontaneously or as a result of treatment

You may not qualify if…

Not English literate or without email and internet access
Macrolide allergy
Pregnancy or lactation
Females of childbearing potential must agree to use an acceptable form of contraception during the treatment period
Chronic use of macrolides, tetracyclines or quinolones Chronic use is defined as 4 or more weeks of continuous use within 6 months of randomization
Asthma symptoms for less than 6 months prior to randomization Asthma symptoms must be present for at least 6 months to exclude patients without true chronic asthma
Unstable asthma requiring immediate emergency care All patients with asthma exacerbations will receive usual urgent or emergency care for asthma and must be improving or stable in the judgment of the treating physician prior to being enrolled
Specified co-morbidities likely to interfere with study assessments or follow up. Excluded comorbidities include:
cystic fibrosis
obstructive sleep apnea requiring CPAP
cardiomyopathy
congestive heart failure
terminal cancer
alcohol or other drug abuse
or any other serious medical condition that, in the opinion of the study physician, would seriously interfere with or preclude assessment of study outcomes or completion of study assessments
Specified medical conditions for which macrolide administration may possibly be hazardous
Patients with acute or chronic hepatitis, cirrhosis or other liver disease, chronic kidney disease, or history of prolonged cardiac repolarization and QT interval or torsades de pointes, are excluded
Specified medications for which close monitoring has been recommended in the setting of macrolide administration Patients taking digoxin, theophylline, warfarin, ergotamine or dihydroergotamine, triazolam, carbamazepine, cyclosporine, hexobarbital or phenytoin are excluded.
If any of these medications are started after randomization and before completion of the 12-week treatment phase, study medication will be discontinued and the patient may remain in the study.
The intent of this protocol is to enroll a broadly generalizable sample of adult patients with physician-diagnosed asthma, either stable persistent or in exacerbation.

Where it is running

ANSR — Peoria, Illinois, United States
AAFP National Research Network — Kansas City, Kansas, United States
RAP - Cleveland Clinic — Cleveland, Ohio, United States
University of Oklahoma Health Sciences Center (OUHSC) and Oklahoma Physicians Resource/Research Network (OKPRN) — Oklahoma City, Oklahoma, United States
Wisconsin Research and Education Network (WREN) — Madison, Wisconsin, United States

Full record on ClinicalTrials.gov

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