跳至主要内容
临床试验/EUCTR2011-003648-31-DE
EUCTR2011-003648-31-DE进行中(未招募)不适用

Pharmacokinetic-pharmacodynamic modeling of the postoperative pain sensation during patient-controlled analgesia with target-controlled infusion of Hydromorphone, taking into account the interaction with intraoperatively administered Sufentanil for elective cardiac surgery - PkPd Hydromorphon-Sufentanil

niversitätsklinikum Erlangen0 个研究点开始时间: 2011年8月18日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Written informed consent
  • Ability to understand the nature of patient-controlled analgesia and other study-specific procedures
  • Elective cardiac surgery with thoracotomy and subsequent stay in the intensive care unit
  • 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 40
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 10

排除标准

  • Use of MAO inhibitors in the last 14 days
  • Chronic alcoholism or drug addiction in medical history
  • Severe obstuctive or restrictive pulmonal disorders in medical history
  • Severe hepatic and renal disorders in medical history
  • Hypothyroidism, prostate hyperplasia, pancreatitis, biliary or renal colic in medical history
  • Pregnant or nursing females

研究者

发起方
niversitätsklinikum Erlangen

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