跳至主要内容
临床试验/NL-OMON35741
NL-OMON35741已完成不适用

Pharmacokinetics and pharmacodynamics of esketamine during longterm sedation of children at the intensive care - PK - PD of esketamine during sedation of children

Academisch Medisch Centrum0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
2 至 17(—)

入选标准

  • 1. Sedation with ketamine and lorazepam with protocol: Sedation and analgesia during artificial respiration > 1 week
  • 2. Presence of an arterial or central line for blood sampling
  • 3. Presence of an Informed Consent

排除标准

  • 1. A contra indication for the use of ketamine:
  • ** Increased intracranial pressure leading to serious risks.
  • ** Hypersensitivity for the farmacon
  • 2. Absence of Informed Consent

研究者

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