Effect of Turmacin supplementation on joint discomfort and functional outcome among healthy volunteers â?? a randomized placebo controlled trial

atural Remedies Private Limited0 个研究点目标入组 90 人开始时间: 待定最近更新: 2021年11月24日

试验速览

暂无简介。

•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.

•1.Having trauma or surgery histories that have affected the knee.
•2.Having a disease that results in bad intestinal absorption
•3.Women of child bearing age who do not wish to use approved birth control methods during study
•4.Being pregnant or breastfeeding.
•5.Allergic or hypersensitive to turmeric
•6.Being participating or having participated in a clinical assay or intervention study within the previous 30 days before inclusion in the study
•7.Being unable to follow the guidelines of the study
•8.Subjects having liver problems (raised ALT, AST), Heart (abnormal ECG / ECHO), kidney problems (raised creatinine), other muscle related problems (raised creatine kinase).
•9.Subjects having neurological disorders
•10.BMI greater than 32 kg/m2
•11. Taking concomitant medication like pain relievers or complements/ multivitamin supplements/ phytotherapeutical products that interfere with the product or outcomes of the study.
•12.Suffering from any kind of arthritic condition viz., autoimmune, infectious in the knee that could mislead the evaluation.

发起方

atural Remedies Private Limited