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临床试验/EUCTR2017-002616-13-NL
EUCTR2017-002616-13-NL招募中1 期

The effect of perioperative intravenous s-ketamine on acute and chronic postoperative craniotomy pain compared to placebo - ESPAI

Maastricht Universitair Medisch Centrum0 个研究点目标入组 62 人开始时间: 2017年12月14日最近更新:
相关药物

试验速览

阶段
1 期
状态
招募中
发起方
入组人数
62

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

性别
All

入选标准

  • - Age > 18 years
  • - Elective resective surgery for drug-resistant temporal lobe epilepsy
  • - Drug-resistant epilepsy, based on: (1) chronic, focal epilepsy; (2) not seizure free with antiepileptic medication; (3) no medication options due to adverse effects
  • - Signed informed consent for trial participation
  • 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 62
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Declined informed consent
  • - Allergy to any of the trial medications
  • - Current chronic pain, such as, but not limiting to, migraine or other headaches.
  • - Chronic pain treatment with use of different kinds of pain medication.
  • - Alcohol, hard- or soft drug abuses
  • - Inability to complete questionnaires or language barrier
  • - History of psychiatric complaints for which treatment was performed
  • - History of craniotomy or subdural electrode implantation

研究者

发起方
Maastricht Universitair Medisch Centrum

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