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临床试验/NL-OMON28894
NL-OMON28894尚未招募不适用

Procedural propofol sedation with ketamine versus alfentanil and remifentanil in patients for cardiac ablation.

Catharina Hospital EindhovenMichelangelolaan 25623 EJ EindhovenThe Netherlands040-2399111www.cze.nl0 个研究点目标入组 120 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
120

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

入选标准

  • Patients were eligible if are: scheduled for treatment of atrial fibrillation with CA under PSA, aged 18 years or older, American Society of Anesthesiology (ASA) class 1 to 3.
  • Patients will be included in this study after given written informed consent before the treatment starts.

排除标准

  • Patients will be excluded from the study if they: are unable to give informed consent, are pregnant, have a known allergy to either study medication, have a know contra-indication to administer either study medication, are scheduled for a repeated procedure, are receiving treatment for neuromuscular or psychiatric disease and have a physical or communicational disorder.

研究者

发起方
Catharina Hospital EindhovenMichelangelolaan 25623 EJ EindhovenThe Netherlands040-2399111www.cze.nl

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