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临床试验/JPRN-UMIN000030501
JPRN-UMIN000030501已完成未知

A clinical study to evaluate the anti-fatigue effect of S-allylcysteine - A clinical study to evaluate the anti-fatigue effect of S-allylcysteine

Soiken Inc.0 个研究点目标入组 24 人开始时间: 2019年4月30日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
Soiken Inc.
入组人数
24

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 60years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Subject receiving a medical treatment for serious renal, hepatic, cardio-vascular, respiratory, endocrine or metabolic disorders or having a medical history of these disorders 2) Subject having the chronic fatigue syndrome (CFS), or subject deemed to have severe fatigue like idiopathic chronic fatigue by the investigator 3) Subject having a medical history of chest pain or syncope 4) Subject having an abnormality in the electrocardiogram 5) Subject having a subjective symptom of low back pain, joint pain or lumber hernia, disease of lower limbs, palpitations 6) Subject who has the possibility of developing allergic symptoms by the test food(gelatin allergy) 7)Subject who has a history of its physical condition getting worse after garlic intake 8)Subject who takes regularly health food containing an ingredient derived from garlic 9) Subject who takes regularly pharmaceuticals or quasi-drugs which having the efficacy for recovery from fatigue or nutrient replenishment in case of physical fatigue 10) Subject who takes regularly Foods with Function Claims labeled the effect of attenuating fatigue sensation 11) Subject who have a seasonal allergic rhinitis (cedar or Japanese cypress pollen) with moderate or severe symptoms 12) Subject having blood sample of 200 ml or more taken within 1 month, or 400 ml or more within 3 months prior to the start of the present study (e.g. donated blood) 13) Subject who took part in another clinical study within 3 months prior to the start of the present study or who is currently taking part in another clinical study 14) Female subjects who is pregnant or lactating, or intending to become pregnant during the study 15) Subject deemed unsuitable by the investigator

研究者

发起方
Soiken Inc.

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