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临床试验/ISRCTN99850066
ISRCTN99850066已完成不适用

Evaluation of efficacy and safety of aceclofenac injection in the treatment of acute lumbago: a randomised comparative open-labeled multi-centric trial

Venus Remedies Limited (India)0 个研究点目标入组 300 人开始时间: 2006年10月3日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
300

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

性别
All

入选标准

  • 1. Patients of either sex, aged over 18 years suffering from acute lumbago (that began less than 48 hours before study entry)
  • 2. Pain intensity more than 50 mm on a 100 mm Visual Analogue Scale (VAS)

排除标准

  • Patients with history of:
  • 1. Recurrent peptic ulcer or duodenal ulcer
  • 2. Gastrointestinal bleeding or other bleeding disorders
  • 3. Significant renal or hepatic impairment
  • 4. Any significant abnormality on preclinical trial screening
  • 5. Pregnant and lactating mothers
  • 6. Patients requiring aspirin at any dose, corticosteroids, anticoagulants, ticlopidine hydrochloride or other drugs affecting platelet function and coagulation, and patients taking hormonal contraceptives or patients allergic to Non Steroidal Anti-Inflammatory Drugs (NSAIDs)

研究者

发起方
Venus Remedies Limited (India)

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