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临床试验/NCT02334358
NCT02334358已完成不适用

A Multi-center, Prospective and Observational Study to Evaluate Long-term Safety and Biodegradability of YVOIRE Classic s Injected Into the Nasolabial Folds

LG Life Sciences1 个研究点 分布在 1 个国家目标入组 503 人开始时间: 2014年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
503
试验地点
1
主要终点
Incidence of Device-related Adverse Events

研究概览

简要总结

To evaluate long-term safety of YVOIRE classic s by incidence of adverse events including injection site local reactions and biodegradability

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects whose age is over 18 years old
  • Subjects whose WSRS grade is equal or greater than 2
  • Subjects must be willing and able to provide written informed consent
  • Subjects who are scheduled to be treated with YVOIRE classic s for facial tissue augmentation to correct the nasolabial folds

排除标准

  • Subjects who are sensitive to hyaluronic acid or any excipients of YVOIRE classic s
  • Subjects who have received permanent implantation (silicone, PAAG, PMMA, CaHA etc) on the nasolabial folds
  • Subjects who have received nonpermanent aesthetic treatments, such as botulinum toxin injection or filler on the nasolabial folds within 9 months before screening
  • Subjects who have received face lifting or plastic surgery on face within 9 months before screening
  • Subjects who have received laser therapy on the nasolabial folds, chemical peeling or peeling on face within 3 months before the screening
  • Subjects who have any skin diseases (including inflammation and skin cancer) or infectious diseases on the injection sites
  • Subjects who tend to have hypertrophic scars
  • Subjects with a history of streptococcal disease, severe allergy or anaphylaxis or bleeding disorders.
  • Women in pregnancy or lactation

结局指标

主要结局

Incidence of Device-related Adverse Events

时间窗: Until subject reaching total biodegradation criterion (WSRS change) ; an expected average of 2 years.

次要结局

未报告次要终点

研究者

发起方
LG Life Sciences
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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