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临床试验/EUCTR2015-000964-33-NL
EUCTR2015-000964-33-NL进行中(未招募)1 期

Dexmedetomidine versus propofol in awake implantation of a neuromodulative system. - DexMedPro

Erasmus Medical Center, Department of Anesthesiology0 个研究点目标入组 74 人开始时间: 2015年7月13日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
74

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

  • - Patients need to be betweem 18 and 65 years
  • -Patients have an indication for implantation of a neuromodulative system
  • 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 74
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • -Hypersensitivity of active part of one of any of the excipients
  • -AV-blok (II or III)
  • -Acute cerebrovascular disease
  • -Pregnancy
  • -Acute epilepsy
  • -Severe liver dysfunction
  • -Use of a beta blocker
  • -Psychologically unstable
  • -Communication problem
  • -Heart rate <60bpm
  • -Allergy for soya or peanuts
  • -Heart failure
  • -Severe heart disease
  • -Electroconvulsive therapy (ECT)
  • -ASA III, IV, V

研究者

发起方
Erasmus Medical Center, Department of Anesthesiology

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