KCT0004384
尚未招募
未知
Efficacy and Safety of laser surgery 'Liposci' procedure in initial validity reduction of abdominal circumference : A Single-blind Randomized Clinical Trial
概览
- 阶段
- 未知
- 干预措施
- 未指定
- 疾病 / 适应症
- Factors influencing health status and contact with health servisces
- 发起方
- WONTECH
- 入组人数
- 20
- 状态
- 尚未招募
- 最后更新
- 6年前
概览
简要总结
暂无简介。
研究者
入排标准
入选标准
- •1\. Adult male or female over 19 years of age.
- •2\. BMI (Body mass index) \= 35 kg/m2
- •3\. If the thickness of the lower abdomen fat measured using Caliper is greater than 2\.5 cm.
- •4\. No other treatment is planned for body contouring or weight loss during this clinical trial.
- •5\. If you agree to keep your weight (within ± 5%) by not changing your diet or lifestyle
- •6\. Voluntarily decided to participate in this clinical trial and gave written consent
排除标准
- •1\. pregnant, nursing, or women planning to conceive within the clinical trial period or who do not agree to the proper use of contraceptives during the clinical trial period.
- •2\. In case of history or related treatment of blood clotting disorder (anti\-platelet, anticoagulant, thrombotic release, aspirin, anti\-inflammatory drugs)
- •3\. If you have experience with esthetic treatment in the treatment area within 12 months prior to the screening, or with surgical treatment to remove abdominal fat (fat\-absorbent, laparotomy, mezzoterapi, etc.)
- •4\. In case there are implanted electrical devices such as pacemaker and defibrillator.
- •5\. Unregulated diabetes or cardiovascular disease
- •6\. For LDL cholesterol \= 190 mg/dL
- •7\. Patient is diagnosed with hepatitis and is in treatment 3 or within 12 months of the end of hepatitis treatment
- •8\. Surgical operation on the surgical site within 18 months of screening
- •9\. If there is a history of skin cancer or pre\-cancerous lesions in the treatment area
- •10\. In case there is a skin condition, such as infection, injury, and scarring, in the area of treatment
结局指标
主要结局
未指定
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