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Otolaryngol Head Neck Surg ; 127(1): 1-6, 2002 Jul.
Article in English | MEDLINE | ID: mdl-12161723

ABSTRACT

OBJECTIVE: The primary objective of this study was to demonstrate the clinical and radiologic efficacy of 5 days compared with 7 days of gemifloxacin therapy in the treatment of acute bacterial rhinosinusitis (ABRS). STUDY DESIGN: In this prospective, double-blind, multicenter, parallel-group study, adult patients presenting with ABRS were randomized to receive gemifloxacin 320 mg once daily for either 5 days (n = 218) or 7 days (n = 203). RESULTS: For the primary efficacy end point, clinical response to therapy at follow-up, 5 days of therapy with gemifloxacin was as effective as 7 days of therapy (per-protocol population; treatment difference 0.44%; 95% confidence interval [CI], -6.54 to 7.41). Five and 7 days of treatment with gemifloxacin were well tolerated. CONCLUSION AND SIGNIFICANCE: The clinical efficacy of gemifloxacin 320 mg daily for 5 days is at least as good as the efficacy of gemifloxacin 320 mg daily for 7 days in the treatment of ABRS.


Subject(s)
Anti-Infective Agents/administration & dosage , Bacterial Infections/drug therapy , Fluoroquinolones , Naphthyridines/administration & dosage , Rhinitis/drug therapy , Sinusitis/drug therapy , Acute Disease , Administration, Oral , Adult , Bacterial Infections/microbiology , Confidence Intervals , Dose-Response Relationship, Drug , Double-Blind Method , Drug Administration Schedule , Female , Follow-Up Studies , Gemifloxacin , Humans , Male , Middle Aged , Probability , Prospective Studies , Rhinitis/complications , Rhinitis/microbiology , Sinusitis/complications , Sinusitis/microbiology , Treatment Outcome
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