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Study on the effect of blood pressure suppression by single intake of test foods

Study on the effect of blood pressure suppression by single intake of test foods - Study on the effect of blood pressure suppression by single intake of test foods

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000053620
Enrollment
16
Registered
2024-02-15
Start date
2024-03-06
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 Adults

Interventions

Single intake of 4g of test food with 100mL of water Single intake of 100mL of water

Sponsors

Healthcare Systems Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Persons who received a sufficient explanation of the purpose and contents of the exam, have the capacity to consent, applied with free will with sufficient understanding, and agreed to participate with a written document 2. Adults who are 18 years old or more and under 65 years old

Exclusion criteria

Exclusion criteria: 1. Persons who have chronic illness, receiving medication, have a serious disease history 2. Persons who are allergic to the test food 3. Persons who usually take a large amount of test food 4. Persons who usually take medicine, specified health food, healthy food and supplements that may affect blood pressure 5. People who have a history of hospitalization for hypertension treatment 6. Persons with systolic blood pressure less than 160 mmHg and diastolic blood pressure less than 100 mmHg 7. Persons who have participated in other tests within the first month before the start of the test, or those who intend to participate in another exam after consenting to this exam 8. Persons who were judged as inappropriate for study participants by the principal investigator 9. Persons who are pregnant, planning or hoping to be pregnant during the study period, breastfeeding

Design outcomes

Primary

MeasureTime frame
Blood pressure (systolic and diastolic blood pressure) change before and after intake.

Secondary

MeasureTime frame
Subjective evaluation of swelling

Countries

Japan

Contacts

Public ContactMari Shimura

Healthcare Systems Co., Ltd. Clinical Research Department

shimura.mari@hc-sys.jp0368092722

Outcome results

None listed

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