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临床试验/JPRN-UMIN000038272
JPRN-UMIN000038272已完成未知

A Multicenter, Post-Market Observational (non-interventional) Study of SUPARTZ in Subjects with Osteoarthritis of the Knee or Periarthritis of the Shoulder - Post-Market Observational Study of SUPARTZ

SEIKAGAKU CORPORATIO0 个研究点目标入组 60 人开始时间: 2019年10月21日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1. Subjects for whom the product is contraindicated according to the Instructions For Use or subjects to whom, in any case, the product is administered not in accordance with the Instructions For Use. 2. Subjects with a history of hypersensitivity due to any ingredients of SUPARTZ.

研究者

发起方
SEIKAGAKU CORPORATIO

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