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Effects of Sage Juice Consumption on Anti-Fatigue and Q0L in Women

Effects of Sage Juice Consumption on Anti-Fatigue and Q0L in Women - Effects of Sage Juice Consumption on Anti-Fatigue and Q0L in Women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000048729
Enrollment
50
Registered
2023-08-01
Start date
2022-09-10
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 women

Interventions

Intake of Saji juice Intake of placebo juice

Sponsors

Finess Co, Ltd.
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: (1) Those who are temporarily fatigued or have low vitality due to a desk-bound job (2) Premenopausal women between the ages of 20 and 50 (3) BMI less than 30 kg/m2 (4) Those with relatively stable menstrual cycles (5) Persons who give written voluntary consent to participate in the study (6) Those who can continue to drink SajiJuice

Exclusion criteria

Exclusion criteria: (1) Those who are currently under medication for iron deficiency anemia (2) Those who are currently receiving medication for some disease. (3) Those who are consuming food products containing the ingredients of this test food or health food products. (4) Subjects with irregular menstruation (5) Persons with serious diseases of glucose metabolism, lipid metabolism, liver function, renal function, heart, circulatory system, respiratory system, endocrine system, immune system, nervous system or psychiatric disorders. (6) Persons with a history of such diseases (6) Persons with a history of abnormal clinical laboratory values that would be considered problematic for study participation (7) Persons who have a disease under treatment or a history of a serious disease that required medication (8) Persons who may develop allergies related to the study (9) Persons who are judged to be unsuitable as subjects based on the results of the lifestyle questionnaire (10) Subjects who are participating in other clinical studies at the time this study is initiated. (11) Pregnant or planning to become pregnant or breastfeeding during the study period (12) Persons who are judged to be unsuitable to participate in the study by the investigator (or study administrator).

Design outcomes

Primary

MeasureTime frame
QOL Questionnaire for Daily Life

Secondary

MeasureTime frame
Blood test related to anemia, temporary fatigue when performing work tasks

Countries

Japan

Contacts

Public ContactNibun Shigenori

EAS inc. Clinical Trial Session

info@eas-ct.jp045-374-3392

Outcome results

None listed

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