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临床试验/JPRN-UMIN000027937
JPRN-UMIN000027937已完成未知

Effect of test supplement on postprandial serum uric acid: A double blinded, placebo controlled, and cross over study - Effect of test supplement on postprandial serum uric acid

FANCL Corporation0 个研究点目标入组 6 人开始时间: 2017年7月5日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
6

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
Male

入选标准

  • 未提供

排除标准

  • 1. Subjects who have been taking foods affecting the study results once a week or more 2. Subjects who have gout in the past or are currently receiving treatment for hyperuricemia or gout (including exercise therapy, dietary guidance) 3. Subjects who are under treatment or have history of diseases (urinary stone, kidney stone, rheumatoid arthritis) which may influence the outcome of the study 4. Subjects who routinely use analgesics (non-steroidal analgesics, steroidal analgesics, etc.). 5. Subjects who have diseases requiring continuous medication, or serious medical history who needed medication therapy 6. Subjects who are under treatment or have a history of serious disease(e.g., diabetes, liver disease, kidney disease, or heart disease) 7. Subjects with allergies to the test food in the study 8. Subjects who have participated in other clinical study within the last one month prior to the current study or are planned to participate in other clinical study after informed consent for the current study 9. Subjects who are judges as unsuitable for the study based on the results of background survey 10. Subjects who are judged as unsuitable for the study by the investigator for other reason

研究者

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