A Phase 3 interventional study of Avelox (Moxifloxacin, BAY12-8039) and Ceftriaxone + Metronidazole in Infection, Intra-abdominal, sponsored by Bayer. Completed at 25 sites in 6 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2014-12-18.
Sponsored by Bayer · Phase 3, Interventional, and Treatment
The purpose of this study is to assess the safety and efficacy of intravenous administration Moxifloxacin (BAY 12-8039) compared to intravenous ceftriaxone and metronidazole for the treatment of patients with complicated intra abdominal infections. In view of the fact that intra abdominal infections are typically polymicrobial and are often treated empirically, the selected antibacterial agent must cover the likely spectrum of bacterial pathogens. Combination antibiotics therapy has been widely used with great success.
6,687 studies on the registry are indexed under Infections; 807 are open to participants now.
This study's enrollment of 364 is above the median of 120 across 4,200 interventional studies indexed under Infections.
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Of its 209 completed or terminated interventional studies of FDA-regulated products, 129 (62%) have results posted.
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Exclusion Criteria:
Drug: Ceftriaxone + Metronidazole
Drug: Avelox (Moxifloxacin, BAY12-8039)
Moxifloxacin 400 mg every 24 h
Ceftriaxone 2 g every 24 h and Metronidazole 500 mg every 12 h
Clinical Response
Time frame: After 10-14 days of treatment
Clinical and bacteriological response
Time frame: During 3-5days of treatment
Bacteriological and radiological response
Time frame: After 10-14 days of treatment
Clinical response at the TOC visit in patients with bacteriological proven intra abdominal infection
Time frame: After 10-14 days of treatment
Mortality attributable to intra abdominal infection
Time frame: 13-28 days
This study is completed, as verified in Dec 2014. You cannot join it, but the record below documents what was studied.
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