A study for verification of oral environment-improving and stress-reducing effects by test-food ingestion - A study for verification of oral environment-improving and stress-reducing effects by test-food ingestion

CPCC Company Limited0 sites30 target enrollmentSeptember 27, 2022

Overview

Phase: 未知
Intervention: Not specified
Conditions: Not specified
Sponsor: CPCC Company Limited
Enrollment: 30
Status: Completed
Last Updated: 2 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

No summary available.

Registry

who.int

Start Date

September 27, 2022

End Date

November 8, 2022

Last Updated

2 years ago

Study Type

Interventional

Sex

All

Investigators

Sponsor

CPCC Company Limited

Eligibility Criteria

Inclusion Criteria

Not provided

Exclusion Criteria

•(1\) Subjects who take steadily (not less than three times a week) in the health\-specific/functional (e.g., reduced coenzyme Q10\-containing)/supplementary/ health foods, which might affect the test results. (2\) Subjects who have taken affecting medicines (e.g., antihistamine/ antidepressant/ antihypertensive/ antiinflammatory/painkiller), and have any difficulty in refraining from taking them during this study. (3\) Subjects who use some kind of oral care product (e.g., mouthwash), and have any difficulty in refraining from using them during this study. (4\) Subjects who have been to the hospital for dental treatment within three months prior to the consent, or those who are now under the treatment (including scaling tartar and plaque). (5\) Subjects who have been diagnosed as dry mouth or Sjogren's syndrome. (6\) Subjects with salivary secretion of no more than 2 g, according to the results of the Saxon tests at the moment of preliminary examination. (7\) Subjects fully realized that their gums are liable to bleed. (8\) Subjects with excessive alcohol intakes. (9\) Subjects who have previous/current medical history of severe cardiac, hepatic, renal or digestive diseases. (10\) Pregnant, lactating, possibly pregnant women during this study. (11\) Subjects having drug/food allergy. (12\) Subjects who are now under other clinical studies with some kind of medicine and/or health food, or partook in those within four weeks before this study, or are going to participate in those after giving informed consent to take part in this study. (13\) Others who have been determined as ineligible for participation, judging from the principal/sub investigator's opinion.