JPRN-UMIN000045597已完成未知
Test for confirmation of absorption of a compound by ingestion of test foods - Test for confirmation of absorption of a compound by ingestion of test foods
R&D Institute, MORINAGA & CO., LTD.0 个研究点目标入组 10 人开始时间: 2021年10月6日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 10
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) People who have difficulty with acidity (2) Those who are currently taking any medication. (3) Those who are scheduled to take medication or receive vaccinations between one week before the first test date and the second test date. (4) Heavy drinkers of alcohol (5) Those who are unable to go to bed and sleep as usual the day before the test day (6) Those who have been told that their blood vessels are too thin or that it is difficult to draw blood more than once (7) Those who are aware that they have severe symptoms such as irregular menstruation, menstrual cramps, or symptoms related to menopausal disorders. (8) Those who have a history or current history of serious diseases of the heart, liver, kidneys, digestive organs, etc. (9) Those who are pregnant, lactating, or intend to become pregnant during the study period. (10) Those with allergies to medicines or food (11) Those who are currently participating in a clinical trial of another drug or health food, and plan to participate in another clinical trial within 4 weeks of the end of the trial, or after consenting to participate in the trial. (12) Those who have donated component blood or 200 mL whole blood since the month prior to the start of the study. (13) Men who have donated 400 mL of whole blood for 3 months prior to the start of the study. (14)Women who have donated 400 mL of whole blood for 4 months prior to the start of the study (15) Men whose total blood collection volume exceeds 1200 mL when the planned total blood collection volume for the study is added to the blood collection volume from 12 months prior to the start of the study (16)Women whose blood volume exceeds 800 mL when the total planned blood volume for the study is added to the blood volume collected 12 months prior to the start of the study. (17) Patients who are judged to be inappropriate for participation in the study by the principal investigator or sub-investigator. Translated with www.DeepL.com/Translator (free version)
研究者
相似试验
已完成
不适用
Absorbency confirmation test of food ingredientsJPRN-UMIN000038580TTC Co., Ltd8
已完成
不适用
Absorbency and efficacy confirmation test of food ingredientsJPRN-UMIN000041787TTC Co., Ltd8
招募中
不适用
The small intestine absorption test using the [1-13C] labeled substance, and a study of bacterial overgrowth in the intestine.JPRN-UMIN000006637Ehime University Graduate School of Medicine100
尚未招募
不适用
An explorative study determining the oral antibiotic drug absorption in patients with short bowel syndrome.Short Bowel SyndromeNL-OMON27546Radboudumc16
已完成
不适用
Assessment of Protein digestibility of legumes by stable isotope based methods in humansCTRI/2017/11/010468The Wellcome Trust Department of Biotechnology India Alliance24