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.
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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