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Clinical Trials/JPRN-UMIN000045663
JPRN-UMIN000045663Completed未知

A study to evaluate the safety of excessive intake of plant extract materials-2 - A study to evaluate the safety of excessive intake of plant extract materials-2

Soiken Inc.0 sites40 target enrollmentStarted: October 23, 2021Last updated:
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Conditions

Trial Snapshot

Phase
未知
Status
Completed
Enrollment
40
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
20years-old to 65years-old (—)
Sex
All

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • •1) Subjects with serious cardio-vascular, hepatic, renal, respiratory, endocrine or metabolic disorders or having a medical history of these disorders 2) Subjects who have the possibility of developing allergic symptoms by the test food 3) Female subjects who are pregnant or lactating, or intending to become pregnant during the study 4) Subjects 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) 5) Subjects who took part in another study within 3 months prior to the start of the present study or who is currently taking part in another study 6) Subjects deemed unsuitable by the investigator

Investigators

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