JPRN-UMIN000010982已完成3 期
A confirmatory study of SI-657 in Patients with Enthesopathy (Lateral Epicondylitis, Patellar Tendinitis, Achilles Tendinitis and Plantar Fasciitis) - A confirmatory study of SI-657 in Patients with Enthesopathy (Lateral Epicondylitis, Patellar Tendinitis, Achilles Tendinitis and Plantar Fasciitis)
KAKEN PHARMACEUTICAL CO., LTD/SEIKAGAKU CORPORATIO0 个研究点目标入组 540 人开始时间: 2013年6月21日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 540
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
- 16years-old 至 75years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1.Patients who received localized injection at the involved limb or any steroid topical treatment within 2 weeks before administration. 2.Patients with acute symptoms (i.e., sprain, injury or surgery) at the affected site. 3.Patients with infectious risk at administration due to their skin disease or infection. 4.Patients, the investigator (or the subinvestigator) considers, inappropriate for entry into the trial.
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