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临床试验/EUCTR2014-002555-26-DK
EUCTR2014-002555-26-DK进行中(未招募)不适用

MEROPENEM and CIPROFLOXACIN DOSING IN THE CRITICALLY ILL PATIENT WITH SEPTIC SHOCK – A SINGLE CENTER PHARMACOKINETIC STUDY

Dept. of Intensive Care Medicine, Copenhagen University Hospital, Rigshospitalet0 个研究点目标入组 50 人开始时间: 2014年6月26日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
50

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

  • Age >18 years and <90 years
  • > Clinical indication for therapy of one of the study antibiotics Meropenem or Ciprofloxacin in patients diagnosed at or during admission to ICU with septic shock.
  • a. Sepsis will be defined as:
  • i. Clinical suspicion of infection and/or Positive culture results
  • ii. Systemic inflammatory response syndrome (SIRS) as defined by 2 or more of the following:
  • iii. Core temperature < 36o C or > 38o C
  • iv. Tachycardia as defined by a heart rate > 90 beats per minute
  • v. Tachypnoea as defined by a respiratory rate greater than 20 breaths per minute OR a PaCO2 less than 32 mmHg during spontaneous ventilation OR the requirement for mechanical ventilation.
  • vi. A white blood cell count > 12 X 109 / L OR < 4 X 109 / L OR greater than 10 % immature (band) forms.
  • b. Septic shock will be defined as:
  • i. Sepsis with persistent hypotension, systolic blood pressure < 90 mmHg or mean arterial pressure < 65 despite adequate fluid resuscitation or
  • ii. Requirement of inotropic support.
  • > Normal renal function as defined by:
  • i. Serum creatinine <170 mmol/L
  • 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 15
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 35

排除标准

  • -Pre-existing renal impairment as defined by: Serum creatinine above normal limits ( defined as >500mmol/L)
  • - Need for renal replacement therapy
  • - History of allergy to study antibiotic
  • - Pregnancy

研究者

发起方
Dept. of Intensive Care Medicine, Copenhagen University Hospital, Rigshospitalet

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