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临床试验/NCT02180516
NCT02180516已完成不适用

Safety and Efficacy of Meloxicam (MOBIC) Compared to Other NSAIDs in Approved Therapeutic Dosages and Routes of Administration in an Observational Cohort Study of Patients With Rheumatoid Arthritis, Osteoarthritis, Lumbago, Scapulohumeral Periarthritis, Neck, Shoulder and Arm Syndrome

Boehringer Ingelheim0 个研究点目标入组 9,984 人开始时间: 2001年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
9,984
主要终点
Incidence for adverse event of gastrointestinal disorder

研究概览

简要总结

Study to assess the safety profile of meloxicam by comparing incidence of gastrointestinal adverse events of meloxicam with that of NSAID in the routine daily therapeutic situation.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients with Indications according to the package insert of the prescribed NSAID

排除标准

  • There is no exclusion criterion, because this Post Marketing Study is an observational study

研究组 & 干预措施

Meloxicam

干预措施: Meloxicam (Drug)

Other NSAIDs

干预措施: Other Non Steroidal Anti-Inflammatory Drugs (NSAIDs) except etodolac (Drug)

结局指标

主要结局

Incidence for adverse event of gastrointestinal disorder

时间窗: up to 6 months

次要结局

  • Incidence for adverse events Perforation, Ulcer and Bleeding (PUB) in the upper gastrointestinal tract(up to 6 months)
  • Incidence for adverse drug reaction of gastrointestinal disorder(up to 6 months)
  • Incidence of adverse events(up to 6 months)
  • Incidence of adverse drug reactions(up to 6 months)
  • Incidence of serious adverse events(up to 6 months)

研究者

申办方类型
Industry
责任方
Sponsor

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