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临床试验/JPRN-UMIN000001807
JPRN-UMIN000001807已完成2 期

Efficacy and Safty of Long Acting Beraprost (TRK-100STP) for Lumbar Spinal Canal Stenosis with Intermittent Claudication :A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial - Phase2 exploratory study of TRK-100STP

KAKEN PHARMACEUTICAL CO., LTD.0 个研究点目标入组 150 人开始时间: 2009年3月30日最近更新:

试验速览

阶段
2 期
状态
已完成
入组人数
150

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
40years-old 至 80years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • (1)Patients who have any complication, which could affect efficacy assessments. (2)Patients who is bleeding or have a tendency to bleed. (3)Patients are allergic to beraprost sodium. (4)Patients have severe disorders. (5)Patients who determined the principal investigator or the sub-investigator to be inadequate to participate in the trial.

研究者

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