A Comparison of Safety and Efficacy of Cefdinir Oral Suspension Versus Azithromycin in Pediatric Subjects With Acute Otitis Media

Completed · Phase 4

Conditions studied: Acute Otitis Media

In brief

To compare the safety and efficacy of cefdinir oral suspension, 7 mg/kg every 12 hours for 5 days, to azithromycin oral suspension 10 mg/kg/day (Day 1) then 5 mg/kg/day (Days 2-5) for a total of 5 days, in children between 6 months and 6 years of age, with AOM.

Key facts

Study ID

NCT00645112

Run by

Abbott

People needed

357

Starts

2003-11-01

Last updated by the study team

2008-03-27

Who can join

Age: 1 and older, up to 6. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Clinical diagnosis, documented by medical history and physical examination, is AOM I 1 week.
• Clinical symptoms include >=1 of the following: Otalgia (earache or pain), this may be expressed as ear pulling or nabbing; Ear fullness; Decreased hearing, this may be based on reports from parents or legally authorized representatives; Discharge from the external auditory canal (following acute perforation of the tympanic membrane).
• At least two (2) of the following signs are present in at least one ear: Full or bulging or perforated tympanic membrane, which may be erythematous (note - since hyperemia may be present in a febrile or crying child, a red tympanic membrane alone is insufficient for the diagnosis of AOM); Loss of tympanic membrane landmarks (opacity of the tympanic membrane); Abnormal tympanic membrane mobility on biphasic pneumatic otoscopy, due to the presence of pus or fluid behind the tympanic membrane and edema of the tympanic membrane. Have evidence of middle ear fluid demonstrated by acoustic reflect tympanometry (ear check) showing values of 3, 4 or 5.
• Generally in good health based on medical history, vital signs, physical exam, and historical laboratory results.
• Subject must be a suitable candidate for oral antibiotic therapy.

You may not qualify if…

• Previous enrollment in this study.
• Enrollment in any other investigational study using unapproved products or unapproved doses; in the previous four weeks prior to study start.
• Hypersensitivity reactions to cefdinir, other cephalosporins, azithromycin, other macrolide and azalide antibiotics, and/or sensitivity to multiple allergens.
• Presence of tympanostorny tubes or otitis externa at Evaluation 1.
• Systemic treatment with any anti-infective agent within 14 days prior to Evaluation 1 or during the study.
• Treatment with a long-acting injectable antimicrobial agent (e.g., penicillin G benzathine) within 4 weeks prior to study drug administration.
• Concomitant infection that requires additional antimicrobial therapy.
• Evidence of chronic, suppurative otitis media.
• Evidence of perforation of the tympanic membrane > 24 hours.
• Evidence of a physiologic, anatomic, or immunologic defect, which would interfere with resolution of this episode of acute otitis media.
• Immunocompromised subject (e.g., neutropenic subjects).
• Presence of a disease, complicating factor (e.g., mastoiditis), or structural abnormality that would preclude evaluation of the subject's therapeutic response.
• Any expectation that treatment with probenecid will be expected during the study drug administration period.
• Known significant renal or hepatic impairment.

Where it is running

• Study site — Columbiana, Alabama, United States
• Study site — Montgomery, Alabama, United States
• Study site — Ozark, Alabama, United States
• Study site — Fresno, California, United States
• Study site — Fresno, California, United States
• Study site — Marietta, Georgia, United States
• Study site — Stone Mountain, Georgia, United States
• Study site — Dubuque, Iowa, United States
• Study site — Bardstown, Kentucky, United States
• Study site — Louisville, Kentucky, United States
• Study site — Owensboro, Kentucky, United States
• Study site — Cadillac, Michigan, United States
• Study site — Kalamazoo, Michigan, United States
• Study site — Portage, Michigan, United States
• Study site — Richland, Michigan, United States
• Study site — Omaha, Nebraska, United States
• Study site — Columbus, Ohio, United States
• Study site — Huber Heights, Ohio, United States
• Study site — Pittsburgh, Pennsylvania, United States
• Study site — Reading, Pennsylvania, United States
• Study site — Sellersville, Pennsylvania, United States
• Study site — Charleston, South Carolina, United States
• Study site — Kingsport, Tennessee, United States
• Study site — Lake Jackson, Texas, United States
• Study site — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

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