JPRN-UMIN000048641已完成Unknown
Trial to confirm the usefulness of pyrroloquinoline quinone disodium salt (PQQ) ingestion - PQQ clinical trial
Kyowa Trial Co., Ltd.0 个研究点目标入组 62 人开始时间: 2023年12月20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
- 62
研究概览
简要总结
A significant difference was observed in the primary outcome.
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20years-old 至 75years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1)Those who meet the diagnostic criteria for sarcopenia 2)Those who have a continuous exercise habit of at least 2 days per week 3)Those who have been attending the hospital for knee, back or other joint pain within 3 months 4)Those with a history of major surgery in the gastrointestinal tract area, such as gastrectomy, gastrointestinal suture, or intestinal resection 5)Those who have difficulty to participate in this study because of conditions i.e., liver, kidney, or cardiac disease, breathing, endocrinology, metabolism, nervous, or conscious disorder, diabetes (determined by JDA), and other diseases 6)Those with history of cardiovascular diseases 7)Those who regularly use amino acids or protein-enriched foods or beverages for the purpose of maintaining physical fitness, improving exercise function, or dieting 8)Those who have allergies related to test food 9)Those with a history or current history of hepatitis or those with circulatory system disease or severe anemia 10)Those who use medicines, health foods and supplements (including "Food for specified health uses", "Foods with function claims" and "Food with nutrient function claims") constantly, excepting those who can stop them at taking of informed consent 11)Previous experience of poor or worsened health after giving a blood sample 12)Blood donations 200 mL or more in the month before the trial or have plans for making a blood donation 200 mL or more during the trial period 13)Participation in another clinical trial, whether ongoing or within the last four weeks 14)Heavy drinkers and smokers 15)Extremely irregular dietary patterns 16)Late night and irregular shift workers 17)Those who do not wish to provide their consent to the details of the trial explained to them in advance 18)Those who judged that examination responsible doctor is not appropriate for this study participation
研究者
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