跳至主要内容
临床试验/PER-094-03
PER-094-03已完成未知

MULTINATIONAL, PROSPECTIVE, RANDOMIZED, DOUBLE-BLIND STUDY TO INVESTIGATE THE EFFECTIVENESS AND SECURITY OF THE INTRAVENOUS / ORAL SEQUENTIAL MOXIFLOXACINE COMPARED WITH INTRAVENOUS CEFTRIAXONE MORE INTRAVENOUS LEVOFLOXACINE FOLLOWED BY ORAL LEVOFLOXACIN, IN THE TREATMENT OF PATIENTS WITH SEVERE PNEUMONIA ACQUIRED IN THE COMMUNITY.

BAYER S.A.,0 个研究点目标入组 0 人开始时间: 2003年12月31日最近更新:

试验速览

阶段
未知
状态
已完成
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Patients 18 years of age or older.
  • All the signs and symptoms of pneumonia.
  • Fine Score> 71
  • Informed written consent obtained from the patient or legal representative.

排除标准

  • Known hypersensitivity to fluoroquinolones, or other quinolones, and / or to beta-lactams, and / or to macrolide antibiotic medications.
  • Female patients who are pregnant or breastfeeding.
  • Antecedents of disease / tendon alteration related to treatment with fluroquinolones.

研究者

发起方
BAYER S.A.,

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