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临床试验/JPRN-UMIN000014278
JPRN-UMIN000014278已完成未知

A clinical study for evaluating the effect of L-citrulline on physical performance - A clinical study for evaluating the effect of L-citrulline on physical performance

Soiken Inc.0 个研究点目标入组 20 人开始时间: 2014年6月16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
20

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
20years-old 至 39years-old(—)
性别
Male

入选标准

  • 未提供

排除标准

  • 1) Subject taking any medical treatment(prescribed a medicine by a doctor) 2) Subject receiving a medical treatment for serious renal, hepatic, cardio-vascular, respiratory, endocrine or metabolic disorders or having a medical history of these disorders 3) Subject having a medical history of a chest pain or swoon career 4) Subject having a subjective symptom of low back pain, arthralgia or lumber hernia, disease of lower limbs, palpitations 5) Subject having an abnormality in the electrocardiogram 6) Subject having the possibilty of developing allergic symptoms by test food 7) 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 8) Subject having the habit of taking a supplement 9) Subject received a serious injury within past 1 year 10) Subject taking part in any sports events during the present study period or within 1 month before and after the period 11) Subject going abroad or having a trip for more than 3 days and 2 nights during the present study 12) Subject having a smoking habit 13) Subject having a seasonal allergy of a cedar or Japanese cypress pollen 14) 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 15) Subject judged to be ineligible by the investigator for other reason

研究者

发起方
Soiken Inc.

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