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临床试验/NCT02183168
NCT02183168已完成3 期

A Randomized, Open Label, 3-arm Evaluation of Efficacy and Safety of Meloxicam Suppository (15mg Daily) and Tablet (15 mg Daily) Compared to Indomethacin Suppository (50 mg Daily) in Patients With Ankylosing Spondylitis

Boehringer Ingelheim0 个研究点目标入组 192 人开始时间: 2001年7月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
192
主要终点
Overall assessment of disease activity by the patient on VAS

研究概览

简要总结

Study to assess the efficacy and safety of meloxicam suppository 15 mg once daily, meloxicam tablet 15 mg once daily compared with Indomethacin suppository (50 mg daily) in patients with ankylosing spondylitis

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Active ankylosing spondylitis (pain rated >= 40 mm on a VAS and increased of at least 30% after nonsteroidal anti-inflammatory drugs (NSAIDs) wash-out)), without peripheral arthritis and inflammatory bowel disease

排除标准

  • 未提供

研究组 & 干预措施

Meloxicam suppository

Experimental

干预措施: Meloxicam suppository (Drug)

Meloxicam tablet

Experimental

干预措施: Meloxicam tablet (Drug)

Indomethacin suppository

Active Comparator

干预措施: Indomethacin (Drug)

结局指标

主要结局

Overall assessment of disease activity by the patient on VAS

时间窗: 6 weeks

Functional Index of ankylosing spondylitis of Dougados

时间窗: 6 weeks

Overall pain during the previous 48 hours assessed on a Visual Analogue Scale (VAS)

时间窗: 6 weeks

次要结局

  • Global efficacy assessed by the investigator (verbal rating scale)(6 weeks)
  • Assessment of Chest expansion(6 weeks)
  • Assessment of Fingers - to - floor test(6 weeks)
  • Duration of morning stiffness(6 weeks)
  • Global efficacy assessed by the patient (verbal rating scale)(6 weeks)
  • Number of study withdrawals due to lack of efficacy(6 weeks)
  • Assessment of Paracetamol consumption(6 weeks)
  • Assessment of Patient status with regard to disease condition(6 weeks)
  • Overall assessment of disease activity by the investigator on a VAS(6 weeks)
  • Evaluation of spinal pain by the investigator (verbal rating scale)(6 weeks)
  • Assessment of Schober test(6 weeks)
  • Assessment of Night pain (verbal rating scale)(6 weeks)
  • Total number of study withdrawals(6 weeks)

研究者

申办方类型
Industry
责任方
Sponsor

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