Treatment of Patients With Acute Sinusitis
- 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
Group Intervention Description Group 1 Avelox (Moxifloxacin, BAY12-8039) -
- Primary Outcome Measures
Name Time Method 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 of Documentation 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
Name Time Method 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 sinusitis Documentation at baseline visit. History and frequency of sinusitis episodes Documentation at baseline visit. Diagnostic procedures and therapeutic options chosen by physicians in daily practice Documentation at baseline visit.