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临床试验/NCT04649138
NCT04649138已完成不适用

Fomepizole Dosing During Continuous Renal Replacement Therapy (CRRT)

Oslo University Hospital1 个研究点 分布在 1 个国家目标入组 11 人开始时间: 2019年6月13日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
11
试验地点
1
主要终点
Measure minimum plasma concentration of fomepizole

研究概览

简要总结

The project is a prospective observation study of patients with suspected or confirmed toxic alcohol poisoning treated with fomepizole and continuous renal replacement therapy (CRRT)

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients (over 18 year) with suspected or confirmed toxic alcohol poisoning treated with fomepizole and CRRT.

排除标准

  • Patients who wish to withdraw from the study

结局指标

主要结局

Measure minimum plasma concentration of fomepizole

时间窗: through study completion, up to 72 hours

Plasma samples will be obtained up to every hour and before fomepizole is given

次要结局

  • Continuous renal replacement therapy (CRRT) clearance of fomepizole(through study completion, up to 72 hours)
  • Determine saturation/sieving coefficient of fomepizole(through study completion, up to 72 hours)

研究者

发起方
Oslo University Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Knut Erik Hovda, MD, PhD

Principal Investigator

Oslo University Hospital

研究点 (1)

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