IRCT20240416061507N1尚未招募4 期
Evaluating the efficacy and safety of Deoxycholic acid injection (Embella®) in reduction of flank fat
Espad Pharmed Co0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 30
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 21 years 至 65 years（—）
- 性别
- All
入选标准
- •Mild to moderate flank fat (clinically proven and based on caliper measurements and ultrasound criteria)
- •Ability to complete the study and follow instructions
- •Informed consent to participate in the study
- •Consent on not performing any other intervention in the flank area during the study period
排除标准
- •Severe medical or psychological conditions that interfere with the study results
- •History of hypersensitivity to components of the product under study
- •Pregnancy and breastfeeding
- •History of previous flank fat treatment
- •Patients prone to intravascular volume reduction
- •Evidence of recent alcohol or drug abuse
- •History of bleeding disorders or recent consumption (less than 3 weeks) of thrombolytic drugs, anticoagulants, platelet inhibitors orNSAIDs
- •History of hypertrophic scarring
- •Infection, inflammation, dermatosis, unhealed wound, cancer or precancerous lesions at the injection site
研究者
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