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Clinical Trials/JPRN-UMIN000023757
JPRN-UMIN000023757
Completed
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 sites20 target enrollmentMay 14, 2018

Overview

Phase
未知
Intervention
Not specified
Conditions
Healthy volunteers
Sponsor
Soiken Inc.
Enrollment
20
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 14, 2018
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 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

Outcomes

Primary Outcomes

Not specified

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