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临床试验/TCTR20220507001
TCTR20220507001Unknown4 期

Efficacy and Safety of High-Intensity, High-Frequency, Parallel Ultrasound Beams for the Treatment of Upper and Lower Facial Laxity: A Pilot Study

Sofwave Medical Ltd.0 个研究点目标入组 30 人开始时间: 2022年5月7日最近更新:
适应症

试验速览

阶段
4 期
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
30 Years 至 50 Years(—)
性别
All

入选标准

  • 1. BMI < 25 kg/m2
  • 2. Participants with mild to moderate severity of upper and lower facial laxity using a comprehensive quantitative 4-point laxity grading scale

排除标准

  • 1. Pregnant or lactating women
  • 2. Having metals in the body or pacemakers or electronic medical devices
  • 3. Severe acne or cystic acne on face
  • 4. Taking oral isotretinoin or oral retinoids in the past 6 months
  • 5. Other skin diseases or having infection at the area of face
  • 6. Immunocompromised patients
  • 7. Treated with botulinum toxin or laser treatment in the past 6 months
  • 8. Treated with filler on face in the past 6 months

研究者

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