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临床试验/ACTRN12612000945820
ACTRN12612000945820招募中4 期

Continuous infusion antipseudomonalbetalactams versus standard short infusions in the treatment of acute infective exacerbations in patients with cystic fibrosis - impact on clinical and microbiological outcomes

Dr Anton Peleg0 个研究点目标入组 120 人开始时间: 2012年9月4日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
120

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • 1) Patients greater than or equal to 18 years of age,
  • 2) Pseudomonas aeruginosa isolated in sputum within the last 12 months,
  • 3) has an acute infective exacerbation, defined by international standards 2 or more of the following in the last 2 weeks:
  • change sputum volume or colour,
  • increased cough,
  • increased dyspnoea,
  • increased malaise, fatigue or lethargy,
  • anorexia or weight loss,
  • decrease in pulmonary function by 10% or more, or
  • new radiographic changes

排除标准

  • 1) patients < 18 yrs of age,
  • 2) patients that do not meet the criteria for an acute infective exacerbation,
  • 3) previous enrolment in the study,
  • 4) concurrent pulmonary embolism, significant haemoptysis, pneumothorax, or respiratory failure,
  • 5) impaired renal function with an estimated creatinine clearance < 60 mls/min,
  • 6) patients allergic to beta-lactam antibiotics,
  • 7) aminoglycoside contra-indicated,
  • 8) intravenous antibiotics in the last 2 weeks, prior to this admission,
  • 9) received more than 24 hours of intravenous antibiotics in this admission,
  • 10) previous lung transplantation,
  • 11) pregnancy or lactation, or
  • 12) inability to consent.

研究者

发起方
Dr Anton Peleg

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