跳至主要内容
临床试验/EUCTR2006-000763-29-LT
EUCTR2006-000763-29-LT进行中(未招募)不适用

Pharmacokinetics, pharmacodynamics and safety of intra-articular multiple doses of 500 mcg icatibant in an uncontrolled 13-week multi-center study in patients with symptomatic knee osteoarthritis - TRICAPEKA

Sanofi-Aventis Deutschland GmbH0 个研究点目标入组 12 人开始时间: 2006年4月13日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
12

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Male and female subjects with painful osteoarthritis of the knee
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Subjects with knee OA of Kellgren & Lawrence grade < II
  • - Age < 18 years
  • - Diagnosis of OA < 3 months (based on the 1986 American College of Rheumatology (ACR) diagnostic criteria
  • - History of inflammatory or infectious joint disease of an origin other than OA
  • - Acute major trauma
  • - Existence of a relevant pain problem at localizations other than the target knee joint (e.g., migraine, low back pain etc., but also bilateral symptomatic knee OA)

研究者

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