NCT03759743已完成不适用
a Randomised, Double Blind, Placebo Controlled Study to Evaluate the Efficacy and Safety of LMT1-48 on Reducing Body Fat in Overweight Subject
Medy-Tox1 个研究点 分布在 1 个国家目标入组 97 人开始时间: 2018年9月4日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 97
- 试验地点
- 1
- 主要终点
- change from baseline fat percentage at 12 week
研究概览
简要总结
The purpose of this study is to evaluate the safety and efficacy of LMT1-48(Probiotics) compared to a placebo in reducing the body fat in overweight subjects
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 19 Years 至 70 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age between 19 and 70 years
- •Overweight (25 kg/m2 ≤ body mass index (BMI) < 30 kg/m2)
排除标准
- •Pregnancy or breast-feeding
- •Unstable body weight (body weight change > 10% within 3 months before screening)
结局指标
主要结局
change from baseline fat percentage at 12 week
时间窗: at baseline and 12-week follow-up
the body composition of the subjects was measured via dual-energy X-ray absorptiometry (DEXA) to determine
次要结局
未报告次要终点
研究者
研究点 (1)
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