A clinical study to evaluate the efficacy of high-blood pressure by continuous ingestion of food containing plant-derived ingredients. ( SME-2021-01-FOSHUS)

A clinical study to evaluate the efficacy of high-blood pressure by continuous ingestion of food containing plant-derived ingredients.(SME-2021-01-FOSHUS) - A clinical study to evaluate the efficacy of high-blood pressure by continuous ingestion of food containing plant-derived ingredients.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000044352

Enrollment

120

Registered

2021-05-27

Start date

2021-05-28

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

None listed

Interventions

Daily intake of test food for 12 weeks Daily intake of control food for 12 weeks

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: (1) Males and females who are -> 20 years old at the time of IC acquisition and <65 years old at the end of the study. (2) Those who can visit to destination medical institution on the scheduled date. (3) Those who have submitted written informed consent after fully understanding the purpose and content of this study.

Exclusion criteria

Exclusion criteria: (1) Those who heavy use of alcohol or smoke (2) Those who continuously ingest foods for specified health use, foods with functional claims, health foods, and foods that may affect blood pressure evaluation. (3) Those who continuously take medicines or quasi-drugs (4) Those who are participating in other study or planning to participate or participated within the past 4 weeks. (5) Those who are: a) heart, liver, or kidney disease (including complications of other diseases) b) having a history of cardiovascular disease c) diabetes d) allergic to test foods e) with systolic blood pressure of 160 mmHg or higher, or diastolic blood pressure of 100 mmHg or higher f) with a BMI of 30 or higher g) having a history or respiratory illness (excluding childhood asthma) (6) Others who are judged inappropriate for participant by the investigator

Design outcomes

Primary

Measure	Time frame
Systolic blood pressure / Diastolic blood pressure	—

Countries

Japan

Contacts

Public ContactNoriko Sekiguchi

SUNTORY MONOZUKURI EXPERT LIMITED HE Center

N_Sekiguchi@suntory.co.jp03-5579-1277

Outcome results