JPRN-UMIN000048862已完成Unknown
Confirmation study of improvement effects by test-food intakes in oral environment - Confirmation study of improvement effects by test-food intakes in oral environment
CPCC Company Limited0 个研究点目标入组 80 人开始时间: 2023年9月10日最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- 入组人数
- 80
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20years-old 至 65years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •(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., antifungal/antibiotic/ antihistamine/antidepressant/ antihypertensive), and have any difficulty in refraining from taking them during this study. (3) 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 (except taking a periodic dental checkup). (4) Subjects equipped with full dentures. (5) Subjects who might cast off their capped teeth during this study, or are planning to be under dental treatment. (6) Subjects who take a daily care of their tongue. (7) Subjects who have been diagnosed as dry mouth or Sjogren's syndrome. (8) Subjects fully realized that their gums are liable to bleed. (9) Subjects with excessive alcohol intakes. (10) Subjects who have previous/current medical history of severe cardiac, hepatic, renal or digestive diseases. (11) Pregnant, lactating, possibly pregnant women during this study. (12) Subjects having drug/food allergy. (13) 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 take part in those after giving informed consent to participate in this study. (14) Others who have been determined as ineligible for participation, according to the principal/sub investigator's opinion.
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