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临床试验/JPRN-UMIN000021801
JPRN-UMIN000021801已完成2 期

Study on efficacy and safety of Hochuekkito for the treatment of partial paralysis as a complication of cerebrovascular disorder - Efficacy of Hochuekkito for "partial paralysis" in patients undergoing rehabilitation

Department of Rehabilitation Tsuruoka Kyoritu Rehabilitation Hospital0 个研究点目标入组 100 人开始时间: 2016年4月6日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
100

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
50years-old 至 80years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • Patients who have any of the following conditions: 1)Insufficient nutrition intake (less than 1,400kcal/day) 2)CRP of 10g/dL or more 3)Grade 2 or severer on the physical disability certificate or Grade 3 or severer certification of long-term care need since before the onset of cerebrovascular disorder 4)Use of any Kampo medicine within 4 weeks before study initiation 5)Serious comorbidities (e.g., hepatic, renal, cardiac, hematological, and metabolic diseases) 6)Any other condition assessed as inappropriate for study participation by the investigator or subinvestigator (hereinafter referred to as "investigators, etc.")

研究者

发起方
Department of Rehabilitation Tsuruoka Kyoritu Rehabilitation Hospital

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