NCT02218788已完成不适用
An Open-label, Retrospective, Postmarketing Study of Safety and Performance of Hydroxytite, a Calcium Hydroxyapatite Based Filler for Facial Soft Tissue Augmentation.
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Panaxia Ltd
- 入组人数
- 218
- 主要终点
- To assess the safety of Hydroxytite (Crystalys) in subjects who received subdermal or deep-dermal injections
研究概览
简要总结
The purpose of this study is to assess the safety and performance of Hydroxytite in all subjects who have received sub dermal or deep dermal injections.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Patient is over 18 years of age
- •Patient received Hydroxytite injection(s).
排除标准
- •Patient declines to participate in the study
结局指标
主要结局
To assess the safety of Hydroxytite (Crystalys) in subjects who received subdermal or deep-dermal injections
时间窗: 6 months
Adverse events or Serious adverse events, Injection site reactions.
次要结局
- Performance(6 months)
研究者
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