JPRN-UMIN000034060已完成未知
Clinical Evaluation of the Efficacy of Carrot Juice on Perennial Allergic Rhinitis of Healthy Subjects - Effects of Carrot Juice on Perennial Allergic Rhinitis
Others0 个研究点目标入组 40 人开始时间: 2018年9月10日最近更新:
适应症
试验速览
- 阶段
- 未知
- 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
- 20years-old 至 59years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1) Subjects who will be treated or take medicine for perennial allergic rhinitis during this study period. 2) Subjects who planning some treatment during this study period. 3) Subjects who intake the medicines, the foods for specified health uses and/or the health foods that are concerned their influence to test results. 4) Pregnant or expected pregnant, planning pregnant during this study period and lactating women 5) Subjects who have current medical history of serious disease. 6) Subjects who have previous medical history of serious disease and be judged unsuitable for this study. 7) Subjects who take medicines such as anti-histamine and anti-allergy. 8) Subjects who cannot take test food and record diary as instructions. 9) Subjects who habitually consume higher amount of alcohol ( > 60 g alcohol/day) 10) Subjects who have non-allergic rhinitis 11) Subjects who cannot eat carrot 12) Subjects with risk of allergy regarding to this study 13) Subjects who are participating in the other clinical tests. Subjects who participated in the other clinical tests within 2-months prior to this study and/or who plan to participate in the other clinical tests. 14) Subjects who donated over 200mL blood and/or blood components within the last one month to this study. (15) Subjects who donated over 400mL blood and/or blood components within the last three month to this study. (16) Females who donated over 400mL blood and/or blood components within the last four month to this study. (17) Males who will be collected over 1200mL blood and/or blood components, when the sampling amounts within the last twelve month are adding to the planned sampling amounts of this study. (18) Females who will be collected over 800mL blood and/or blood components when, the sampling amounts within the last twelve month are adding to the planned sampling amounts of this study. 19) Subjects who are judged unsuitable for this study by principal investigator and doctors.
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