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Treatment of Patients With Acute Sinusitis

Completed
Conditions
Acute Bacterial Sinusitis
Interventions
Registration Number
NCT00930488
Lead Sponsor
Bayer
Brief Summary

For each patient, an initial visit and at least one follow-up visit at the end of treatment should be documented by the treating physician in the case report form.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
6777
Inclusion Criteria
  • Any patient with a diagnosis of acute bacterial sinusitis treated with Avelox® - in accordance with the local production information.
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Exclusion Criteria
  • Those specified in the local product information - contraindications and precautions must be considered.
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Group 1Avelox (Moxifloxacin, BAY12-8039)-
Primary Outcome Measures
NameTimeMethod
Evaluation of potential benefits of an antibacterial therapy with Avelox® (moxifloxacin) in patients with acute bacterial sinusitis to whom this treatment was prescribed. Especially the time to improvement and resolution of clinical signs and symptoms ofDocumentation at baseline and at at least one follow-up visit. Evaluation of therapy outcome at last follow-up visit at end of therapy (approximately after 7 days).
Secondary Outcome Measures
NameTimeMethod
Evaluation of tolerability and safety of Avalox® in daily practice were investigated.Evaluation of therapy outcome at last follow-up visit at end of therapy (approximately after 7 days).
Patient characteristics in acute bacterial sinusitisDocumentation at baseline visit.
History and frequency of sinusitis episodesDocumentation at baseline visit.
Diagnostic procedures and therapeutic options chosen by physicians in daily practiceDocumentation at baseline visit.
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