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Study of the effect of continuous intake of test food on blood ketone concentration.

Study of the effect of continuous intake of test food on blood ketone concentration. - Study of the effect of continuous intake of test food on blood ketone concentration.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000042953
Enrollment
24
Registered
2021-01-13
Start date
2021-01-14
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

Take the test food (high content) once a day Take the test food (low content) once a day Take placebo food once a day

Sponsors

IMEQRD inc.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged between 20 and 40 years at the time of informed consent 2. Japanese male or female 3. BMI of over 20.0 to under 25.0 4. Those who can input electronic diary with smartphone/PC 5. Those who can understand the contents of the study and provide written consent before study based on their free will

Exclusion criteria

Exclusion criteria: Subjects who 1. are currently receiving any types of medicines and/or Chinese medical treatment (except for the drugs taken as needed) 2. are on diet and exercise therapy under the supervision of a doctor 3. have serious liver, kidney, heart, respiratory, endocrine or metabolic diseases. 4. are or were going on diet such as carbohydrate restriction within one month 5. are currently using quasi-drugs, foods for specified health use, health foods and supplements (those who can stop after obtaining consent are acceptable) 6. have a current or previous history of drug and/or food allergies (those who may have allergic symptoms to the test food) 7. Donated component blood or 200ml of whole blood within one month before the study 8. Men who donate 400ml of whole blood from 3 months before the study or women who donates 400ml of whole blood within 4 months before the study 9. have participated in or are currently participating in other clinical trials within one month before obtaining consent, or those who are planning to participate during the study period 10. are currently pregnant or breastfeeding or those who want to become pregnant during the test period 11. consume alcohol excessively (alcohol equivalent 60g or more / day) 12. have smoking habits 13. have an irregular diet, or irregular life rhythms (work in shifts, work late at night etc.) 14. are judged by the investigator to be unsuitable for participating in this study

Design outcomes

Primary

MeasureTime frame
Blood ketone concentration

Secondary

MeasureTime frame
Weight, body fat, BMI

Countries

Japan

Contacts

Public ContactYoshitada Hira

IMEQRD Co., Ltd. Planning and Sales Department

clinical-trial@imeqrd.co.jp03-6704-5968

Outcome results

None listed

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