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A verification study of improvements in the immune activation: an open trial

A verification study of improvements in the immune activation: an open trial - A verification study of improvements in the immune activation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000027372
Enrollment
10
Registered
2017-05-17
Start date
2017-05-18
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 Japanese adults

Interventions

Duration: 4 weeks Test beverage: Kiseisui Dose and direction: Drink 30 mL before the dinner *If you forget to drink the test beverage drink it between after dinner to before going to bed

Sponsors

ORTHOMEDICO Inc.
Lead Sponsor
Seishin-kai Medical Association Inc, Takara Medical Clinic
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Japanese people who are 40 or more to less than 70 years old with experiencing fatigue 2. Those who are considered as appropriate for the study by the physician 3. Within 2, Priority selection is made in the order of II: warning zone, III: observation zone, and IV: safety zone, in immunological grade at baseline, and V: sufficiently high and I: critical zone are excluded

Exclusion criteria

Exclusion criteria: 1. At least one previous medical history or under the treatment of malignant tumor, heart failure or myocardial infarction 2. Currently under the treatment for either cardiac arrhythmia, hepatic disorder, renal disorder, cerebrovascular disorder, rheumatism, diabetes mellitus, dyslipidemia, hypertension or other chronic diseases 3. Those who use or take "Foods for Specified Health Uses" and "Foods with Functional Claims" in daily 4. Those who are smokers 5. Currently taking medicines and/or herbal medicines 6. Those who are allergic to medicines, milk, beans, orange, and/or other food products 7. Those who are pregnant, breast-feeding, and plan to become a pregnant 8. Those who had participated another clinical test for three months when you signed the informed consent form for this trial 9. Others considered as inappropriate for the study by the physician

Design outcomes

Primary

MeasureTime frame
Scoring of immunological vigor *Assess at 0 and 4 weeks after consuming

Secondary

MeasureTime frame
Immunity test T lymphocyte age, T cells, CD4+T cells / CD8+T cells ratio, naive T cells, naive T cells / memory T cells ratio, B cells, NK cells, CD4+T cells, CD8+T cells, CD8+CD28+T cells, memory T cells *Assess at 0 and 4 weeks after consuming

Countries

Japan

Contacts

Public ContactNaoko SUZUKI

ORTHOMEDICO Inc. R&D Department

nao@orthomedico.jp03-3818-0610

Outcome results

None listed

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