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临床试验/JPRN-UMIN000023757
JPRN-UMIN000023757已完成未知

A study to evaluate the effect of multi-supplement intake on attenuating fatigue sensation - The effect of multi-supplement intake on attenuating fatigue sensation

Soiken Inc.0 个研究点目标入组 20 人开始时间: 2018年5月14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
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 food allergy (gelatin) 4) Subject having a medical history of chest pain or syncope 5) Subject having an abnormality in the electrocardiogram 6) Subject having a subjective symptom of low back pain, arthralgia or lumbar hernia, disease of lower limbs, palpitations 7) Subject who regularly takes medicine or quasi-drugs having the efficacy on recovery of fatigue or nutrition disorder at physical fatigue 8) Subject who regularly takes processed food containing ingredients known to attenuate fatigue sensation 9) Subject who regularly takes food containing large amounts of carotenoid 10) 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) 11) 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 12) Female subject who is pregnant or lactating, or intending to become pregnant during the study 13) Subject deemed unsuitable by the investigator

研究者

发起方
Soiken Inc.

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