跳至主要内容
临床试验/EUCTR2011-003895-35-BG
EUCTR2011-003895-35-BG进行中(未招募)不适用

A Phase III, Randomized, Multicenter, Double Blind, Double-Dummy Parallel-Group, Comparative Study to Determine the Efficacy, Safety, and Tolerability of Ceftazidime Avibactam (CAZ-AVI) Plus Metronidazole Versus Meropenem in the Treatment of Complicated Intra Abdominal Infections (cIAIs) in Hospitalized Adults

AstraZeneca AB0 个研究点目标入组 583 人开始时间: 2012年5月18日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
583

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 18 to 90 years of age inclusive
  • - Female patient is authorized to participate if at least one of the following criteria are met:
  • (a) Surgical sterilization
  • (b) Age =50 years and postmenopausal as defined by amenorrhea for 12 months or more following cessation of all exogenous hormonal treatments (c) Age <50 years and postmenopausal as defined by documented LH and FSH levels in the postmenopausal range PLUS amenorrhea for 12 months or more following cessation of all exogenous hormonal treatments
  • (d) Patient has a negative serum pregnancy test (serum ß-human chorionic gonadotropin [ßhCG]) within 1 day prior to study entry, and agrees to use highly effective contraception methods during treatment and for at least 7 days after last dose of IV study therapy.
  • - Intraoperative/postoperative enrollment with confirmation (presence of pus within the abdominal cavity) of an intra-abdominal infection associated with peritonitis
  • - Confirmation of infection by surgical intervention within 24 hours of entry: evidence of systemic inflammatory response; physical findings consistent with intraabdominal
  • infection; supportive radiologic imaging findings of intraabdominal
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 466
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 117

排除标准

  • - Patient is diagnosed with traumatic bowel perforation undergoing surgery within 12 hours; perforation of gastroduodenal ulcers undergoing surgery within 24 hours. Other intraabdominal processes in which primary etiology is not likely to be infectious
  • - Patient has abdominal wall abscess or bowel obstruction without perforation or ischemic bowel without perforation
  • - Patient has suspected intraabdominal infections due to fungus, parasites, virus or tuberculosis
  • - Patient is considered unlikely to survive the 6 to 8 week study period or has a rapidly progressive or terminal illness, including septic shock that is associated with a high risk of mortality

研究者

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