Avelox (Moxifloxacin, BAY12-8039)
DrugPatients with a diagnosis of acute bacterial sinusitis who take moxifloxacin
NCT Number: NCT00930488
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.
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Observational
Many Locations, Austria
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients with a diagnosis of acute bacterial sinusitis who take moxifloxacin
Time frame: 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).
Time frame: Evaluation of therapy outcome at last follow-up visit at end of therapy (approximately after 7 days).
Time frame: Documentation at baseline visit.
Time frame: Documentation at baseline visit.
Time frame: Documentation at baseline visit.
Bayer
Industry
Treatment of Patients With Acute Sinusitis in Daily Practice
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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