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临床试验/NL-OMON48377
NL-OMON48377已完成不适用

Respiratory effects of tapentadol and oxycodone assessed by pharmacokinetic-pharmacodynamic and response surface modeling in healthy volunteers - SURF study

eids Universitair Medisch Centrum0 个研究点目标入组 24 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
24

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

年龄范围
18 至 99(—)

入选标准

  • Healthy volunteers of either sex aged 18-38 years

排除标准

  • - Presence of health issues including presence or history of any psychiatric,
  • medical or neurologic disorder that may interfere with the current study (eg.
  • neuropathic pain conditions);
  • - Presence or a history of illicit drug use or excessive alcohol
  • consumption (>21 units per week),
  • - Known allergies to study medication.
  • - A positive drug screen on the day of screening or on any of the study
  • - Participation in another trial in the 3 months before enrolment,
  • - Use of medication on a regular basis (e.g. pain medication),
  • - Inability to fast for at least 8 hours prior to study treatment
  • administration,
  • - Pregnancy or lactation,
  • - Inability to communicate with the research team
  • - elective surgery during the study period.

研究者

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