跳至主要内容
临床试验/NL-OMON26606
NL-OMON26606招募中不适用

Rotation from subcutaneous infusion to transdermal administration of fentanyl: A validation ofcurrent practice

Erasmus MC0 个研究点目标入组 30 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
Erasmus MC
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

入选标准

  • Age > 18 years
  • Able to understand the written information and able to give informed consent.
  • Current treatment with subcutaneous fentanyl and planned to rotate to transdermal
  • To ensure steady-state kinetics, patients must have been treated with
  • subcutaneous fentanyl for at least 40 hours prior to the rotation and have been
  • treated with a stable fentanyl dose at least 20 hours prior to the rotation This way,
  • fentanyl pharmacokinetics are at steady-state.

排除标准

  • Patients that use short-acting fentanyl via the oral, (oral mucosal, sublingual),
  • intranasal or subcutaneous administration route 12 hours prior to the rotation will
  • be excluded as this influences the pharmacokinetic profile of the subcutaneous
  • administration. This implicates that patients will be prescribed oral short acting
  • oxycodone or morphine 12 hours before rotation as these are mostly used next to
  • treatment with transdermal fentanyl.
  • Patients that use strong CYP3A4 inhibitors or inducers will be excluded as the
  • model did not account for the influence of strong CYP3A4 inhibition or induction on
  • fentanyl pharmacokinetics while the effects have been shown in multiple studies
  • Patients that are rotated using a dose conversion ratio other than 1:1 will also be

研究者

发起方
Erasmus MC

相似试验