EUCTR2019-003900-10-BE进行中（未招募）1 期
Pharmacokinetics of intravenous meropenem administered over 12 hours at 2g 3x/d every 6 hours
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 20
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
- 性别
- All
入选标准
- •- Adult > 18 years old (male or female)
- •- non-pregnant woman / breastfeeding
- •- Non-obese (BMI <30)
- •- Normal renal function (clearance >or = 60ml/min)
- •- Requiring meropenem treatment for a bacterial infection requiring a treatment duration of at least 10 days.
- •- The studied dosing regimen will be administered during the non-acute phase of the infection, i.e. 2 days before the planned discontinuation of treatment or discharge of the patient with HAD-OPA.
- •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 16
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 4
排除标准
- •- pregnant woman
- •- creatinine clearance below 60ml/min
研究者
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