ISRCTN38432711已完成不适用
A double blind randomised placebo controlled trial to compare two doses of a mineral supplement and a herbomineral combination in alleviating the symptoms of osteoarthritis of the knee
Vedic Lifesciences (India)0 个研究点目标入组 107 人开始时间: 2005年3月7日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 107
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. Ambulatory adults of either sex of greater than 20 years of age
- •2. OA of the knee diagnosed as per radiologic examination and the American Rheumatology Association (ARA) functional classification (II or III) or Kellgren-Lawrence Classification of grade II or grade III
- •3. Functional assessments of overall pain of at least 50 mm on a 100 mm Visual Analogue Scale
排除标准
- •1. Osteoarthritis of grade I or grade IV
- •2. ARA functional class I or IV
- •3. Any arthritis other than OA
- •4. Arthroscopy of either knee for the past year
- •5. Intraarticular steroids for the last 3 months or hyaluronic acid in the last 9 months
- •6. Pregnant or lactating women
- •7. Evidence of severe renal, haematologic disease or severe cardiac insufficiency as revealed by laboratory investigations and other tests
- •8. Unwilling to come to regular follow up visits for the duration of the study
- •9. Moderate to severe peripheral neuropathy
- •10. Any condition that the investigator feels does not allow participation in the study
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