KCT0002238招募中未知
Efficacy and Safety of ATEon reducing body weight and body fat of overweight subjects; A 12week, Randomized, Double-blind, Placebo-Controlled Clinical Trial
Dong Il Pharmtec0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 20(Year) 至 60(Year)（—）
- 性别
- All
入选标准
- •1)Subject who voluntarily agree to participate and signs informed consent form
- •2) 20 years= Age = 60years)
- •3) 25kg/m^2= BMI =29.9kg/m^2
排除标准
- •1) Subjects with severe cerebrovascular disease, cardiac disease (If that patient's clinical status is stable, they can participate in the clinical trial according to investgator) within recent 6 months
- •2) Subjects for uncontrolled hypertension(systolicBP = 160 mmHg or diastolicBP = 100 mmHg)
- •3) Subjects with diabetes(use of hypoglycemic agent or insulin)or fasting blood glucose = 126 mg/dL or random blood glucose = 200 mg/dL
- •4) Subjects with TSH(thyroid-stimulating hormone) = 0.1 uIU/ml or = 15 uIU/ml
- •5) Subjects with Creatinine = 2 times the upper limit of normal
- •6) Subjects with AST or ALP = 3 times the upper limit of normal
- •7) Subjects with complaint of severe gastrointestinal symptoms such as heartburn, dyspepsia
- •8) Subjects who take the medicine that can affect the state of weight change (uptake inhibitors, appetite suppressant, health functional food for diet, antidepressants, ß- blocker, diuretics, contraceptives, steroid, and female sex hormone) within recent 1 months
- •9) Participation in commercial diet program within the 3 months prior to screening
- •10) Participation in any clinical trial within the 1 month prior to screening or have a plan to participate in other clinical trial
- •11) Subjects who get hospitalization, medications or rehabilitation treatments for Alcohol disorders, cardiovascular disease, disorder of central nervous system
- •12) Subjects with the musculoskeletal disorders or restricted physical activity
- •13) Women who are pregnant of lactating or planning to pregnant
- •14) Subjects which in the opinion investigator could affect preclude evaluation of response
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