JPRN-UMIN000046540已完成Unknown
A validation study of changes in salivary volume by one-time using an oral massaging device - A validation study of changes in salivary volume by one-time using an oral massaging device
CPCC Company Limited0 个研究点目标入组 16 人开始时间: 2023年1月11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
- 16
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
- 30years-old 至 80years-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., antihistamine/ antidepressant/antihypertensive), and have any difficulty in refraining from taking them during this study. (3) Subjects who use some kind of imitation of the test device (e.g., an electric toothbrush equipped with supersonic vibration, oral care products) habitually, 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 (except taking a periodic dental checkup). (5) Subjects fully realized that their gums are liable to swell up and bleed. (6) Subjects equipped with full dentures, or being in the process of straightening their teeth. (7) Subjects who have previous/current medical history of severe cardiac, hepatic, renal, digestive or oral diseases. (8) Subjects who are now under other clinical tests with some kind of medicine and/or health food, or took part 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. (9) Pregnant, possibly pregnant, and lactating women. (10) Subjects having latex-related allergy. (11) Others who have been determined as ineligible for participation, according to the principal/sub investigator's opinions.
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