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临床试验/JPRN-UMIN000026192
JPRN-UMIN000026192已完成未知

Examination about the confirmation of the efficacy at change from brand-name sustained-release oxycodone to generic sustained-release oxycodone. - Examination about the confirmation of the efficacy at change from brand-name sustained-release oxycodone to generic sustained-release oxycodone.

Mitoyo General Hospital0 个研究点目标入组 20 人开始时间: 2017年2月22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
20

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
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • Change in basal dose within two weeks before the entry, Increases or decreases in frequency of the rescue dose within two weeks before the entry, Judged inappropriate by the doctor

研究者

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