跳至主要内容
临床试验/TCTR20210520003
TCTR20210520003招募中4 期

Effectiveness and safety of absorbable mesh suture for treatment of lower face laxity

Edencolors (Thailand) Co., Ltd.0 个研究点目标入组 40 人开始时间: 2021年5月20日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
40

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 55 Years(—)
性别
All

入选标准

  • 1. Thai healthy volunteers aged 30-55 years
  • 2. Body mass index < 30 kg/m2
  • 3. Patients with mild to moderate facial laxity
  • 4. No underlying disease, not taking anti-inflammatory drug, antiplatelet drug, vitamin C, or vitamin E

排除标准

  • 1. Patients who are pregnant, lactating, and postpartum within 3 months
  • 2. Patients with history of polydioxanone, xylocaine, and adrenaline allergy
  • 3. Patients with other skin diseases, or having infection at the area of face
  • 4. Immunocompromised patients
  • 5. Patients with hypertrophic scar or keloid
  • 6. Patients with history of regular smoking
  • 7. Patients treated with botulinum toxin or laser on the face in the past 6 months
  • 8. Patients treated with filler or mesh suture on the face in the past 12 months

研究者

发起方
Edencolors (Thailand) Co., Ltd.

相似试验