| Unique ID issued by UMIN | UMIN000060130 |
|---|---|
| Receipt number | R000068595 |
| Scientific Title | A study to confirm the effects of continued intake of test food consumption on oral function in children |
| Date of disclosure of the study information | 2026/06/30 |
| Last modified on | 2025/12/15 13:51:32 |
A study to confirm the effects of continued intake of test food consumption on oral function in children
A study to confirm the effects of continued intake of test food consumption on oral function in children
A study to confirm the effects of continued intake of test food consumption on oral function in children
A study to confirm the effects of continued intake of test food consumption on oral function in children
| Japan |
N/A
| Not applicable | Child |
Others
NO
This study aims to examine the changes in oral function in children due to the continued intake of the test food.
Efficacy
oral function index
Interventional
Single arm
Non-randomized
Open -no one is blinded
Uncontrolled
1
Prevention
| Food |
Oral ingestion of the test food for 4 weeks
| 6 | years-old | <= |
| 9 | years-old | >= |
Male and Female
Child
(1) Healthy male and female aged 6 to 9 years at the time point of acquiring the informed consent.
(2) Those who do not currently have dental care affecting their occlusion.
(3) Those who do not currently have braces.
(4) Those whose first molars have erupted.
(5) Those who are able to eat the test food twice daily.
(6) Those with a body weight of 16.0 kg or more at the time informed consent is obtained.
(7) Those who have received explanation and understood about this study, and who can consent to the content on the informed consent documents.
(8) Those who are judged by the investigator that they have no problem participating in the study.
Parent
(9) Parents of healthy male and female aged 6 to 9 years at the time point of acquiring the informed consent.
(10) Those who can cooperate with diary and questionnaire
(11) Those who have received explanation and understood about this study, and who can consent to the content on the informed consent documents.
(1) Those who have a history of medication, hospitalization, or surgery within a year.
(2) Those who have or suspected infectious disease such as COVID-19, or who are in close contact with such a disease on study entry.
(3) Those who are currently on any medical treatments, or who are planning some kind of treatments during the study period.
(4) Those who cannot eat chewing soft candy.
(5) Those who have allergy in medicine, foods. (Especially gelatin).
(6) Those who are unable to come to the venue on the day of the examination.
(7) Those who have participated in other clinical trials within 3 months prior to the date of consent, are currently participating in a clinical trial of another drug or health food, or are scheduled to participate in another clinical trial after consent to participate in this trial.
(8) Those who judged by the principal investigator to be unsuitable for participation in the study.
70
| 1st name | Noriyuki |
| Middle name | |
| Last name | Nishikawa |
Morinaga & Co., Ltd.
R&D institute
230-8504
2-1-1, Shimosueyoshi, Tsurumi-ku, Yokohama
045-571-6140
n-nishikawa-ie@morinaga.co.jp
| 1st name | Itaru |
| Middle name | |
| Last name | Aoyama |
Morinaga & Co., Ltd.
R&D institute
230-8504
2-1-1, Shimosueyoshi, Tsurumi-ku, Yokohama, Kanagawa
045-571-6140
i-aoyama-af@morinaga.co.jp
Morinaga & Co., Ltd.
Morinaga & Co., Ltd.
Profit organization
Japan Conference of Clinical Research
1-13-23 Minamiikebukuro Toshima-ku Tokyo
03-6868-7022
jccr-info@jccr.jp
NO
| 2026 | Year | 06 | Month | 30 | Day |
Unpublished
Preinitiation
| 2025 | Year | 09 | Month | 18 | Day |
| 2025 | Year | 09 | Month | 18 | Day |
| 2026 | Year | 01 | Month | 17 | Day |
| 2026 | Year | 03 | Month | 14 | Day |
| 2025 | Year | 12 | Month | 19 | Day |
| 2025 | Year | 12 | Month | 15 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000068595