JPRN-UMIN000050090已完成Unknown
Verification research of oral environment-improving effects by test-food consumption - Verification research of oral environment-improving effects by test-food consumption
CPCC Company Limited0 个研究点目标入组 40 人开始时间: 2024年1月24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
- 40
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
- 18years-old 至 70years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •Subjects - - (1) who take steadily (over 3 times a week) in affecting health-specific/functional (e.g., reduced coenzyme Q10, L. reuteri)/supplementary/health foods, (2) who have taken affecting medicines (e.g., anti-biotic/fungal/histamine/hypertensive), and have any difficulty in refraining from taking them during this research, (3) who use an oral care product (e.g., mouthwash), except for toothbrush/paste, and have any difficulty in refraining from using them during this research, (4) who have been to the hospital for dental treatment within 3 months prior to the consent, or those who are now under the treatment (including scaling tartar and plaque), (5) with salivary secretion of less than 2 g at pre-test, (6) who have been diagnosed as dry mouth or Sjogren's syndrome, (7) fully realized that their gums are liable to bleed, (8) equipped with full dentures, (9) with smoking (including no smoking less than 1 year), (10) with excessive alcohol intakes, (11) who have previous/current medical history of severe cardiac, hepatic, renal or digestive diseases, (12) with pregnancy, possibly one, or lactating, (13) having drug/food allergy, (14) who are now under other clinical studies with medicine or health food, or partook in those within 4 weeks before this research, (15) who donated over 0.2 L of their blood and/or blood components within a month to this research, (16) who donated his whole blood (0.4 L) within the last 3 months to this research, (17) who donated her whole blood (0.4 L) within the last 4 months to this research, (18) who will be collected in total of his blood (1.2 L) within the last 12 months, after adding the blood amounts planning to be sampled in this research, (19) who will be collected in total of her blood (0.8 L) within the last 12 months, after adding the blood amounts planning to be sampled in this research, (20) who have been determined as ineligible for participation, judging from the principal/sub investigator - - .
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