JPRN-UMIN000044864尚未招募未知
Efficacy verification of a halitosis-preventive mouthwash on oral malodorous reduction - Efficacy verification of a halitosis-preventive mouthwash on oral malodorous reduction
CPCC Company Limited0 个研究点目标入组 20 人开始时间: 2021年7月14日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 20
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 are continuously taking medicines that may affect the test results, except applying a nasal spray and eye drops. (2) Subjects who have any spots with not less than 7 mm of probing pocket depth. (3) Subjects who are undergoing dental treatment for tooth decay, gingivitis, etc., or ones having tooth decay. (4) Subjects equipped with partial/full dentures. (5) Subjects being in the process of straightening their teeth. (6) Subjects who have any tooth defecting, or coming off. (7) Subjects having a severe medical history of dry mouth symptom, Sjogren's syndrome, or systemic illness. (8) Subjects who have previous and/or current medical history of serious diseases (e.g., heart, liver, kidney, digestive organ). (9) Females who are pregnant, lactating, or possibly pregnant. (10) Subjects who are taking medicine, foods with functional claims, health foods, and oral care products (mouthwash, etc.) that may affect the improvement of oral function. (11) Subjects with an extremely irregular dietary habits or lifestyle (e.g. alternative work schedule, graveyard shift). (12) Subjects who take excessive alcohol. (13) Subjects who are allergic to drugs or foods. (14) Subjects who are participating or have been participated to the other clinical tests with some kind of medicine/food within the last 4 weeks before this trial, or planning to join those after giving informed consent. (15) Others who have been determined as ineligible for participation, according to the principal/sub investigator's opinion.
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