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A study to evaluate the effect of intake of the supplement on the blood flow, fatigue in wome

Not Applicable
Conditions
Healthy adult
Registration Number
JPRN-UMIN000032730
Lead Sponsor
TTC Co., Ltd.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
Female
Target Recruitment
20
Inclusion Criteria

Not provided

Exclusion Criteria

(1) Subjects who routinely use food or medicine containing of functional substance (2) Subjects who performs an act for the improvement of the blood flow, the fatigue, stress, and the quality of the sleep (3) Subjects who use the warm cream (4) Night and day shift worker or manual laborer (5) Subjects who has a disease under treatment or are judged to that medical treatment are necessary by the doctor (6) Subjects who has under treatment or a history of sleep apnea syndrome or is strongly suspected of sleep apnea syndrome (7) Subjects who has had a diagnosis of chronic fatigue syndrome (8) Subjects who has under treatment or a history of serious disease(e.g., diabetes, liver disease, kidney disease, or heart disease) and disease to affect the adrenal cortical hormone secretion (9) Smokers (10) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire and other questionnair (11) Subjects having possibilities for emerging allergy related to the study (12) Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on preliminary examination (13) Subjects who have participated in other clinical study within the last one month prior to the current study or are planned to participate in other clinical study after informed consent for the current study (14) Subjects who are planned to become pregnant after informed consent for the current study or are pregnant or lactating (15) Subjects who are judged as unsuitable for the study by the investigator for other reason

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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