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A study to evaluate the anti-fatigue effect of plant extract material

A study to evaluate the anti-fatigue effect of plant extract material - A study to evaluate the anti-fatigue effect of plant extract material

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000041848
Enrollment
120
Registered
2020-10-10
Start date
2020-10-10
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy volunteers

Interventions

Sponsors

Soiken Inc.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Healthy males and females aged 20- 65 years 2) Subjects who perceive fatigue sensation in daily life 3) Subject whose BMI is 25 kg/m2 or more and less than 30 kg/m2 4) Subject whose HbA1c is 6.0 % or more and less than 6.5 % (for 10 people of each group) 5) Subjects receiving a sufficient briefing of the objective and content of the present study, fully understanding and agreeing to voluntarily participate in the study and being able to personally sign a written informed consent

Exclusion criteria

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 with chronic fatigue syndrome (CFS) , or subjects deemed to have severe fatigue such as idiopathic chronic fatigue by the investigator 3) Subjects who take regularly pharmaceuticals or quasi-drugs which having the efficacy for recovery from fatigue or nutritional supplements during physical fatigue 4) Subjects who take regularly Foods with Function Claims labeled the effect of attenuating fatigue sensation 5) Subjects who have the possibility of developing allergic symptoms by the test food 6) Female subjects who are pregnant or lactating, or intending to become pregnant during the study 7) 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) 8) 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 9) Subjects deemed unsuitable by the investigator

Design outcomes

Primary

MeasureTime frame
VAS(fatigue sensation)

Secondary

MeasureTime frame
Chalder fatigue scale, POMS2 Japanese Adult Short version, OSA sleep inventory MA version, St. Mary's Hospital sleep questionnaire, Munich ChronoType questionnaire, autonomic nervous function evaluation, blood test, body weight, waist circumference, BMI

Countries

Japan

Contacts

Public ContactKota Watanabe

Soiken Inc. R&D Division

watanabe_kota@soiken.com06-6871-8888

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026