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Sensory evaluation of flavor after intake of the test food

Sensory evaluation of flavor after intake of the test food - Sensory evaluation of flavor after intake of the test food

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000060281
Enrollment
20
Registered
2026-01-07
Start date
2026-01-20
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

When the subjects visit the study site, they will consume a single dose of the test product. They will then verbally report their impressions of taste, texture, and other sensory attributes (sensory e

Sponsors

Other
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Male and female subjects aged >=20 years and <80 years at the time of obtaining informed consent. Subjects who have received a sufficient explanation of the purpose and procedures of this study, have the capacity to provide consent, voluntarily agree to participate after fully understanding the study, and are able to provide written informed consent for participation in this study.

Exclusion criteria

Exclusion criteria: 1) Subjects with a known allergy to the investigational product ingredients (wheat, soybeans, or beef). 2) Pregnant or breastfeeding subjects. 3) Subjects who have difficulty consuming the investigational product due to oral/dental disorders, gastrointestinal disorders, or other reasons. 4) Subjects with a history of, or current, serious disease(s) of the liver, kidney, heart, lung, blood, or other organ/system. 5) Subjects with serious concomitant gastrointestinal disease(s) and/or a history of serious gastrointestinal disease. 6) Subjects with a body mass index (BMI) >= 35 kg/m2. 7) Subjects whose habitual alcohol consumption exceeds 60 g/day in terms of pure alcohol equivalent. 8) Subjects who are continuously taking medications that may affect this study. 9) Subjects who are currently receiving medical treatment for a disease and whose treatment is judged to potentially affect the study results or safety. 10) Subjects deemed inappropriate for participation in this study by the principal investigator for any other reason.

Design outcomes

Primary

MeasureTime frame
flavor

Countries

Japan

Contacts

Public ContactTakahiro Matsuda

Nissin Foods Holdings Co., Ltd. Global Innovation Research Center

takahiro.matsuda@nissin.com0426967833

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026