Maxillary Sinusitis
Conditions
Keywords
Maxillary Sinusitis, Infection
Brief summary
The purpose of this study is to evaluate the effectiveness and safety of a once-daily administration of 750 milligrams levofloxacin (an antibiotic) for five days, in treating bacterial sinus infections.
Detailed description
Acute bacterial sinusitis is a common diagnosis for which an antibiotic is prescribed in outpatients. Some types of bacteria that cause sinusitis are resistant to penicillin and certain other classes of antibiotics, but may be treatable with the antibiotic levofloxacin. This will be an open-label, multi-center, non-comparative clinical trial involving outpatients with protocol-defined acute bacterial sinusitis suitable for treatment with oral antibiotics. At the Preliminary Visit, a sinus radiograph will be obtained to confirm the clinical diagnosis of sinusitis, and the Investigator will perform a nasal exam. Sinus puncture and placement of an indwelling sinus catheter into an affected maxillary sinus will be performed on all eligible patients at the first visit. Patients meeting the study criteria will receive 750 milligrams levofloxacin tablets once daily for 5 days. The primary objective is to establish the rate and extent of bacteriological eradication, defined as eradication of pathogens from the maxillary sinus, and to establish the effectiveness and safety of once-daily 750 milligrams levofloxacin for the treatment of acute bacterial sinusitis in adults. Levofloxacin 750 milligram tablet orally once a day for 5 days
Interventions
DRUGlevofloxacin
Sponsors
PriCara, Unit of Ortho-McNeil, Inc.
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Clinical signs and symptoms of acute maxillary sinusitis for 5 to 28 days * Visible nasal purulence evident on physical examination * CT scan or standard sinus x-ray (Waters' projections) performed within 5 days prior to the first dose of study drug, showing total sinus opacification or an air-fluid level * Agree to a maxillary sinus puncture and catheter placement * If female, using birth control
Exclusion criteria
* Chronic sinusitis * Need for hospitalization or intravenous antibiotics * History of head, neck, or nasal cancer or surgery * Previous allergy, serious adverse reaction to, or failed therapy with, levofloxacin or any other member of the quinolone class * Presence or history of serious complications of sinusitis * Previous antimicrobial therapy within 7 days of Study Entry
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time to bacteriological eradication, defined as the complete eradication of original strain(s) from the sinus, by the 5th day of levofloxacin treatment. | — |
Secondary
| Measure | Time frame |
|---|---|
| Efficacy: Clinical response on Day 5 and at the Post-Therapy Visit (Days 12-19); plasma and sinus aspirate concentrations on Days 2-4; levels of inflammatory mediators on Days 0-5. Safety: Adverse events, vital signs, and clinical laboratory tests. | — |
Outcome results
None listed