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A study for the effect of intake of ONO-SR/AST-DA on sleep

A study for the effect of intake of ONO-SR/AST-DA on sleep - A study for the effect of intake of ONO-SR/AST-DA on sleep

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000041059
Enrollment
80
Registered
2021-07-15
Start date
2020-07-12
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 adult

Interventions

Sponsors

TTC Co., Ltd
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Healthy males and females from 20 to 64 years of age (2) A person with a score of 6 or more on Pittsburgh Sleep Questionnaire

Exclusion criteria

Exclusion criteria: 1. Subjects who are currently receiving medication, dietary guidance, or exercise therapy 2. Subjects who perform an act for the improvement of the fatigue, the quality of the sleep, and stress 3. Subjects who were under treatment or have a history of serious diseases 4. Subjects who have history of mental illness, chronic fatigue syndrome, insomnia 5. Subjects who are under treatment or a history of sleep apnea syndrome or are strongly suspected of having sleep apnea syndrome 6. Subjects with nocturnal urination 7. Subjects who are likely to cause skin irritation due to electrode adhesive pads 8. Subjects who have a disease that requires constant medication, subjects with serious diseases that require medication, and subjects with a history of serious diseases 9. Subjects who perform an act for the improvement of the fatigue, the quality of the sleep and stress 10. Subjects who constantly use food richly containing involvement ingredient 11. Subjects who engage in manual labor 12. Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire 13. Subjects who plan to travel abroad or travel abroad during the research period, or who plan to travel on long domestic business trips or domestic trips for more than one week in a row 14. Subjects who have experienced abnormal clinical test values or cardiopulmonary function and have been judged to have problems participating in the study 15. Subjects at risk of developing allergy in relation to the study 16. Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on preliminary examination 17. Subjects who have participated in other clinical study within the last one month prior to the current study 18. Subjects who are planned to become pregnant after informed consent for the current study or are pregnant or lactating. 19. Subjects who are judged as unsuitable for the study by the investigator for other reason

Design outcomes

Primary

MeasureTime frame
Quality of sleep measured by electroencephalograph

Countries

Japan

Contacts

Public ContactShingo Yamamichi

TTC Co., Ltd. Clinical Research Planning Department

s.yamamichi@ttc-tokyo.co.jp03-5459-5329

Outcome results

None listed

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