JPRN-UMIN000027767已完成未知
A clinical study for evaluating the efficacy of seasoning containing functional ingredients on the suppression of the elevation of postprandial serum triglyceride. (Randomised, placebo controlled crossover study) - A clinical study for evaluating the efficacy of seasoning containing functional ingredients on the suppression of the elevation of postprandial serum triglyceride.
CPCC Company, Limited0 个研究点目标入组 16 人开始时间: 2017年6月21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
- 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
- 20years-old 至 60years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •(1) Individuals who use oral medication, supplements and/or functional foods affecting lipid metabolism (2) Individuals who are pregnant or breast-feeding, or have the will of pregnancy during the study period. (3) Individuals who are suffered from or under treatment of serious disease (e.g., heart disease, liver disease, kidney disease, and/or digestive disease) (4) Individuals who are under treatment of alcohol dependence (5) Individuals who are extremely irregular in eating habits (6) Individuals who declare the allergy symptoms against drugs and/or foods (7) Individuals who are participating in other clinical trials of drugs or health food, who participated in the last 4 weeks, or who are willing to participate after giving the informed consent. (8) Individuals who have donated over 200 mL of blood and/or blood component within the last one month prior to the current study (9) Males who have donated over 400 mL of blood and/or blood component within the last three months prior to the current study (10) Females who have donated over 400 mL of blood and/or blood component within the last four months prior to the current study (11) Males whose total blood collection volume exceeding 1200 mL within the last twelve months prior to the current study (include the blood collection volume of the current study) (12) Females whose total blood collection volume exceeding 800 mL within the last twelve months prior to the current study (include the blood collection volume of the current study) (13) Individuals who are judged as unsuitable for the study by the investigator for the other reasons
研究者
相似试验
已完成
不适用
A clinical study for evaluating the efficacy of soft drink containing reduced type of indigestible dextrin on the suppression of the elevation of postprandial serum triglyceride. -Randomised double-blind placebo-controlled trialHealthy adultJPRN-UMIN000022015KSO Corporation90
已完成
不适用
A clinical study for evaluating the efficacy of soft drink containing reduced type of indigestible dextrin on the function of intestinal regulation to subjects having tendency toward constipation. -Randomised double-blind placebo-controlled trialHealthy adultJPRN-UMIN000021665KSO Corporation50
进行中（未招募）
不适用
Investigating the potential clinical benefit of Selumetinib in re-sensitising advanced iodine refractory differentiated thyroid cancer to radioiodine therapy.EUCTR2015-002269-47-GBSheffield Teaching Hospitals NHS Foundation Trust60
尚未招募
2 期
Ayurvedic management of hyperactive childreCTRI/2022/07/044380Sri Dharmasthala Manjunatheshwara College of Ayurveda and Hospital
尚未招募
3 期
Ayurveda Management Of Acute Excerbation Of Tamaka Shwasa(Bronchial Asthma) in ChildreCTRI/2023/08/056084SDM College of ayurveda and hospital Hassan