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临床试验/JPRN-UMIN000020503
JPRN-UMIN000020503已完成未知

Effect of supplement containing N-acetyl glucosamine, proteoglycan and lutein, on knee joint symptoms. - a randomized, double blind, placebo-controlled study - - Effect of supplement containing N-acetyl glucosamine, proteoglycan and lutein, on knee joint symptoms.

Soiken Inc.0 个研究点目标入组 80 人开始时间: 2016年7月1日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
Soiken Inc.
入组人数
80

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
30years-old 至 64years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1)Subjects having a medical history of rheumatism 2)Subjects who have leg pain or numbness 3)Subjects who have injury of semi-lunar disc or the other knee joint disease 4)Subjects receiving treatment for osteoarthritis 5)Subject receiving treatment for serious liver, renal, cardio-vascular, respiratory, endocrine, or metabolic disorders 6)Subject presenting known allergy or history of hypersensitivity to gelatin, crab and salmon 7)For female subject: pregnancy or breast feeding, or possibility of pregnancy, or intention to be pregnant during the study 8)Subject having blood sample of 200 ml or more taken (e.g., donated blood) within 1 month, or 400 ml or more within 3 months prior to the start of the present study 9)Subject who took part in another clinical trial within 3 months prior to the start of the present study or who is currently taking part in another clinical trial 10)Subject deemed unsuitable by the investigator

研究者

发起方
Soiken Inc.

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