ACTRN12616000741482已完成未知
A randomised placebo controlled clinical trial on the efficacy of Caralluma supplement for anxiety and stress in healthy adults over eight weeks
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- RDC Global
- 入组人数
- 117
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 75 Years（—）
- 性别
- All
入选标准
- •Participants will be included for assessment if they self-report mild-moderate anxiety (BAI >9<30), are not diagnosed with depression or a mood disorder, are otherwise healthy, and have given written informed consent.
排除标准
- •Participants will be excluded if they:
- •have a known hypersensitivity to herbal drugs, or nutritional supplements;
- •have been diagnosed with hypertension and are receiving medication;
- •have a medical condition which, in the opinion of the investigator, makes them unsuitable or deemed unhealthy (including a BMI > 30);
- •have currently or have a history of chronic alcohol and/or drug abuse;
- •have participated in any other clinical trial during last 30 days;
- •are currently participating in another clinical trial;
- •have been diagnosed with a mood disorder;
- •have minimal or severe anxiety on the Beck Anxiety Inventory (<10, or > 29);
- •suffered severe PMS with mood or pain that would change during the study;
- •suffered from any neurological disorder;
- •are taking supplements that impact mood or appetite (e.g., St John’s Wort, leptin);
- •are already taking Caralluma.
研究者
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