跳至主要内容
临床试验/CTRI/2009/091/000794
CTRI/2009/091/000794已完成3 期

Comparative, Randomized, Open Label, Parallel, Multicentric Study for Efficacy and Safety of Lornoxicam+ Eperisone versus Lornoxicam in Management of Cervical Spondylosis.

Hetero Labs Limited0 个研究点目标入组 230 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
入组人数
230

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

入选标准

  • a) Male or female patients
  • b) Between 20-65 years of age
  • c) Willing to give written informed consent and willing to comply with trial protocol.
  • d) Out patients with diagnosis of cervical spondylosis.
  • e) Patients with at least 40 mm pain rating on VAS scale.
  • f) Patient and / or physician?s global assessment of arthritic condition as fair, poor or very poor.
  • g) Patients not on any anti-inflammatory or other therapy in the past 2 weeks known to affect the study outcome.

排除标准

  • a) Pregnant and lactating women
  • b) Patients with H/O any drug allergy
  • c) Unwilling to comply with the protocol requirements
  • d) Patients with gastro-intestinal disease, peptic ulcer,
  • bleeding disorder and fecal blood loss.
  • e) Patients with cardiac, hepatic, renal dysfunction and
  • haemopoetic disorder
  • f) Patients with hypertension
  • g) Patients deemed ineligible by the investigator

研究者

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