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临床试验/JPRN-UMIN000027901
JPRN-UMIN000027901已完成2 期

Examination on an influence of a test food product on knee joint pain - Examination on an influence of a test food product on knee joint pain

HUMA R&D CORP0 个研究点目标入组 200 人开始时间: 2017年6月26日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
200

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

年龄范围
40years-old 至 75years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1.Currently seeing a doctor for treatment of knee joint pain 2.Currently in treatment with medication 3.Presence or previous history of allergy to medication and/or food (especially, shrimps and crabs) 4.Presence or previous history of a severe disorder(s) such as diabetes, a circulatory disease, a hepatic disease, a renal disease, or a cardiac disease 5.Currently in treatment of rheumatism 6.Previous history of knee surgery 7.Plan to undergo medical treatment on knees during the study 8.Underwent an intraarticular injection of hyaluronic acid within two weeks before the selection or intraarticular injection of steroids within three months before the selection 9.Diagnosed with a bone or joint-related diseases such as a bone fracture or a sprain within the past three months 10.Regular intake of a health food product that contains hyaluronic acid, glucosamine, chondroitin sulfate, quercetin glycoside, vitamin D, or amino-acid formulation, and the intention of consuming the product during the study 11.Regular intake of medication with an influence on the evaluation of this study (particularly, a pharmaceutical product that contains glucosamine, chondroitin sulfate, vitamin D, or amino-acid formulation, or a pharmaceutical product for treatment of osteoporosis) 12.Regular use of an assistive cane 13.Regular intake of warfarin (product names: Warfarin, Warin, Arefarin, Warfarin, etc.) for treatment of cerebral infarction, a cardiac disease, or the like 14.Nursing or pregnant, or desired to become pregnant during the study 15.Presence or previous history of psychiatric visits for depression, a sleep disorder, etc. 16.Determined by the investigator to be unsuitable for enrollment in this study

研究者

发起方
HUMA R&D CORP

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