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临床试验/JPRN-UMIN000027976
JPRN-UMIN000027976已完成未知

Evaluation of the efficacy of yokukansan for postoperative delirium - Evaluation of the efficacy of yokukansan for postoperative delirium

Tottori University Hospital0 个研究点目标入组 140 人开始时间: 2017年7月3日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
140

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

年龄范围
75years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • Patients with past history of hypersensitivity to yokukansan or anchusan Patients diagnosed with pseudoaldosteronism Patients diagnosed with heart failure Patients with a history of rhabdomyolysis Patients diagnosed with interstitial pneumonia Patients diagnosed with liver failure Patients who cannot start oral administration early after surgery, such as esophageal cancer patients Patients with mood disorder, schizophrenia, schizoaffective disorder, alcoholism, drug addiction Patients determined to be unable to join the clinical trial

研究者

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