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Effects of a Granule Containing Fermented Soba Extract (neo-FBS) on the Decrease of Blood Pressure

Effects of a Granule Containing Fermented Soba Extract (neo-FBS) on the Decrease of Blood Pressure - Effects of a Granule Containing Fermented Soba Extract (neo-FBS) on the Decrease of Blood Pressure

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000024229
Enrollment
54
Registered
2016-10-01
Start date
2016-10-22
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

Normal high blood pressure or Grade 1 hypertension

Interventions

Oral ingestion of the test products containing fermented soba extract (2g per a day
8 weeks) Oral ingestion of the test products containing fermented soba extract (2g per a day
8 weeks) Oral ingestion of the placebo not containing fermented soba extract (2g per a day

Sponsors

Laboratory of Cell Applied Technologies, Co
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Males and females aged 30-70 years 2) Individuals who are healthy and are not receiving treatment of disease 3) Individuals who are high normal blood pressure (SBP: 130-140mmHg and/or DBP: 85-90mmHg) and Grade 1 hypertension (SBP: 140-160mmHg and/or DBP: 90-100mmHg) 4) Individuals whose written informed consent has been obtained 5) Individuals judged appropriate for the study by the principal

Exclusion criteria

Exclusion criteria: 1) Individuals who are sensitive to a food containing soba and test product or other foods, and medical products 2) Individuals who are receiving treatment of serious hepatopathy, kidney damage, heart disease and hematological disease 3) Individuals who have a habit of smoking 4) Individuals who had a habit to ingest health-promoting foods, foods for specified health uses, health foods, or supplements in the past 3 months or will ingest those foods during the test period 5) Individuals who participated in other clinical studies in the past three months 6) Individuals who are or are possibly pregnant, or are lactating

Design outcomes

Primary

MeasureTime frame
Blood pressure, pulsation (Week 0, Week 4, Week 8, Week 12)

Countries

Japan

Contacts

Public ContactMasanori Inoue

Laboratory of Cell Applied Technologies, Co Director

info@l-cat.co.jp044-979-1622

Outcome results

None listed

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