CTRI/2018/03/012367已完成1 期
Tolerability and efficacy of moderately high dose Turmacin supplementation on joint discomfort among healthy volunteers â?? open label single arm pilot study
atural Remedies Private Limited0 个研究点目标入组 15 人开始时间: 待定最近更新:
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 15
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
- •1.All consenting adults aged between 18 and 65 years judged by Investigator to be in general good health on the basis of medical history
- •2.No knee joint discomfort/pain at rest;
- •3.Must achieve a knee joint discomfort/pain score of at least >= 40 mm on visual analogue scale (VAS) for pain after 10 minutes of brisk walk on the stepmill equipment.
排除标准
- •1.Subjects having liver problems (raised ALT, AST), Heart (abnormal ECG / ECHO), kidney problems (raised creatinine), other muscle related problems (raised creatine kinase).
- •2.Subjects having neurological disorders
- •3.BMI greater than 32 kg/m2
- •4.Taking concomitant medication like pain relievers or complements/ multivitamin supplements/ phytotherapeutical products that interfere with the product or outcomes of the study.
- •5.Suffering from any kind of arthritic condition viz., autoimmune, infectious in the knee that could mislead the evaluation.
- •6.Having trauma or surgery histories that have affected the knee.
- •7.Having a disease that results in bad intestinal absorption
- •8.Women of child bearing age who do not wish to use approved birth control methods during study
- •9.Being pregnant or breastfeeding.
- •10.Allergic or hypersensitive to turmeric
- •11.Being participating or having participated in a clinical assay or intervention study within the previous 30 days before inclusion in the study
- •12.Being unable to follow the guidelines of the study
研究者
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