跳至主要内容
临床试验/NCT00612885
NCT00612885已完成不适用

Post Marketing Surveillance to Assess the Safety and Efficacy of Mobic® (Meloxicam) Intramuscular Injection (7.5mg ~ 15mg, q.d.) up to 3 Days (in Case of Need for Prolonged Treatment, Switch to Mobic® Capsule Therapy Was Possible) in Korean Patients With Osteoarthritis and Rheumatoid Arthritis (KFDA Regulatory Requirement PMS)

Boehringer Ingelheim1 个研究点 分布在 1 个国家目标入组 425 人开始时间: 2004年3月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
425
试验地点
1
主要终点
Incidence of adverse events

研究概览

简要总结

The main objective of this PMS study was to monitor and assess the safety of Mobic® intramuscular injection (7.5mg ~ 15mg, q.d.) up to 3 days (in case of need for prolonged treatment, switch to Mobic® capsule therapy was possible) in Korean patients with osteoarthritis and rheumatoid arthritis.

研究设计

研究类型
Observational

入排标准

年龄范围
15 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Incidence of adverse events

时间窗: up tp 3 day

Efficacy assessment by the treating physician

时间窗: up to 3 day

Combined efficacy, safety and tolerability assessment by the treating physician

时间窗: up tp 3 day

次要结局

未报告次要终点

研究者

申办方类型
Industry

研究点 (1)

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