跳至主要内容
临床试验/EUCTR2004-004988-30-IE
EUCTR2004-004988-30-IE进行中(未招募)不适用

PHARMACOKINETICS AND ANALGESIC EFFICACY OF LAEVOBUPIVACAINE, FENTANYL AND CLONIDINE FOR POSTOPERATIVE PARAVERTEBRAL ANAESTHESIA.

Mater Misercordiae Hospital - Department of Anaesthesia0 个研究点目标入组 80 人开始时间: 2005年1月19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
入组人数
80

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
Female

入选标准

  • Patients presenting for breast surgery for cancer, who are not day cases and do not have contraindications for paravertebral analgesia will be approached.
  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Paravertebral analgesia refused or contraindicated
  • Active psychiatric illness
  • Allergy to any of the proposed drugs

研究者

发起方
Mater Misercordiae Hospital - Department of Anaesthesia

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