Efficacy of Short-Course Antimicrobial Treatment for Children With Acute Otitis Media and Impact on Resistance

Alejandro Hoberman

Status and phase: Terminated; Phase 2

Conditions: Acute Otitis Media

Treatments: Drug: Amoxicillin-Clavulanate, 5 days; Drug: Amoxicillin-Clavulanate, 10 days

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT01511107

AI2009058 (Other Identifier)

10-0083

Details and patient eligibility

About

The investigators will study whether, in young children with acute otitis media (AOM), shortening length of antibiotic treatment as a strategy for reducing antimicrobial resistance provides satisfactory clinical outcome. This is a Phase 2b multicenter, randomized, double-blind, placebo-controlled clinical trial in 600 children aged 6 through 23 months comparing the efficacy of consistent reduced-duration antimicrobial treatment (5 days) with that of consistent standard-duration treatment (10 days) for each episode of AOM developing during a single respiratory season (October 1 through May 31).

Full description

Eligible subjects will be randomized at the enrollment visit and will have a telephone call in the course of therapy, and a subsequent visit at the end of therapy. Thereafter, they will be followed through the end of the respiratory season, and their parents will be encouraged to bring their child when concerned about a potential recurrence of AOM. At each recurrence subjects will receive the treatment regimen (either standard- or reduced-duration) to which they were randomized at study entry (consistent treatment strategy).

The recruitment of eligible children with AOM of varying degrees of severity from various primary care practices in 2 separate geographic regions, i.e. Western Pennsylvania and Kentucky, representing urban, suburban and rural demographics will enhance generalizability of study findings and encourage translation to clinical practice.

Enrollment: 520 patients

Sex: All

Ages: 6 to 23 months old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Aged 6 through 23 months

2. Have evidence of AOM defined as:

   • recent (within 48 hours) onset of signs and symptoms as described in the Acute Otitis Media - Severity of Symptoms (AOM-SOS) Scale AND a score of ≥3 at the time of enrollment on the AOM-SOS scale
   • middle ear effusion evidenced by the presence of at least 2 of the following:
   • decreased or absent mobility of the tympanic membrane
   • yellow or white discoloration of the tympanic membrane
   • opacification of the tympanic membrane

   AND

   • acute inflammation evidenced by one of the following:
   • 1+ bulging of the tympanic membrane with either intense erythema or otalgia
   • 2+ or 3+ bulging of the tympanic membrane

3. Has received at least 2 doses of pneumococcal conjugate vaccine

4. Parent has provided informed consent

Exclusion criteria

1. Toxic appearance [capillary refill >3 seconds, systolic blood pressure <60 mm Hg];
2. Inpatient hospitalization
3. Clinical or anatomical characteristics that might obscure response to treatment (tympanostomy tubes in place, cleft palate, or Down syndrome)
4. Sensorineural hearing loss (unilateral or bilateral)
5. Serious underlying systemic problems that might obscure response to infection (cystic fibrosis, neoplasm, juvenile diabetes)
6. Concomitant infection that would preclude evaluation of the response of the child's AOM to study product (pneumonia, periorbital cellulitis)
7. Acute wheezing exacerbation which may require treatment with systemic corticosteroids
8. Known renal or hepatic dysfunction or insufficiency
9. History of amoxicillin-clavulanate-associated cholestatic jaundice
10. Immune dysfunction or receipt of immunosuppressive therapy; chronic gastrointestinal conditions (i.e., malabsorption, inflammatory bowel disease)
11. Co-medications (systemic corticosteroids, more than one dose of systemic antimicrobial therapy within 96 hours, receipt of any investigational drug or vaccine within 30 days)
12. Hypersensitivity to penicillin, amoxicillin or amoxicillin-clavulanate, or phenylketonuria or known hypersensitivity to aspartame
13. Unable to complete study, or no access to phone
14. Previously enrolled in this study or currently enrolled in another study

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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520 participants in 2 patient groups

Amoxicillin-Clavulanate, 10 days

Active Comparator group

Description:

amoxicillin-clavulanate, 90/6.4 mg/kg/day, 2 divided doses, 10 days

Treatment:

Drug: Amoxicillin-Clavulanate, 10 days

Amoxicillin-Clavulanate, 5 days

Other group

Description:

amoxicillin-clavulanate, 90/6.4 mg/kg/day, 2 divided doses, 5 days plus placebo, 2 divided doses, 5 days

Treatment:

Drug: Amoxicillin-Clavulanate, 5 days