Healthy adults
Conditions
Interventions
Duration: 8 weeks Test material: FFC Pairogen 180 ml Tree times/day (540 ml/day)
Duration: 8 weeks Test material: bottled water 500 ml One bottle per day (500 ml/day)
Sponsors
ORTHOMEDICO, Inc.
Seishin-kai Medical Association Inc, Takara Medical Clinic.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: a) Healthy adults, who feel fatigue daily b) Persons who are between 40 and 60 years old
Exclusion criteria
Exclusion criteria: a) Persons who have previous medical history of heart failure or myocardial infarction b) Patients being treated for at least one of following diseases; atrial fibrillation, cardiac arrhythmia, hepatic disorder, renal disorder, cerebrovascular disorder, rheumatism, diabetes mellitus, dyslipidemia, hypertension, and other chronic disease c) Persons who take medicines, herbal medicines, or dietary supplements d) Persons who are allergic to medicines, or foods related to the test material of this trial e) Pregnant women, lactating women, or women who want to get pregnant during the trial period f) Persons who have been enrolled in the other clinical trials within last 3 months before the agreement for the participation to this trial g) Persons who are judged not suitable to participate in this trial by physician.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Oxidative stress and antioxidant potential potential anti oxidant (PAO) serum total antioxidant status (STAS) diacron-reactive oxygen metabolites (d-ROMs) bioantioxidant power (BAP) 8-hydroxy-2'-deoxyguanosine (8-OHdG) propanoyl lysine (PRL) hexanoyl lysine (HEL) | — |
Secondary
| Measure | Time frame |
|---|---|
| microarray analys8s of miRNA (performed to the part of participants) Questionnaires (Likert scale) Blood test Urianalysis Physical examinations | — |
Countries
Japan
Contacts
Public ContactNaoko SUZUKI
ORTHOMEDICO, Inc. R&D department
Outcome results
None listed