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临床试验/NCT01639053
NCT01639053进行中(未招募)不适用

U.S. Postapproval Study of Sientra Silicone Gel Breast Implants

Sientra, Inc.1 个研究点 分布在 1 个国家目标入组 5,498 人开始时间: 2012年4月最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
Sientra, Inc.
入组人数
5,498
试验地点
1
主要终点
Long-term safety of Sientra Silicone Gel Breast Implants in women

研究概览

简要总结

This is a ten-year postapproval study to evaluate the long-term clinical performance of Sientra Silicone Gel Breast Implants under general conditions of use in the postmarket environment.

研究设计

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

入排标准

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

入选标准

  • Genetic female with US residency
  • Is at least 18 years old for primary or revision reconstruction or 22 years old for primary or revision augmentation
  • Agrees to Sientra study requirements

排除标准

  • Has an active infection anywhere in body
  • Has active cancer without adequate treatment
  • Currently pregnant or nursing
  • Has any condition or diagnosis that, in the investigator's opinion, would negatively affect ability to complete study requirements
  • If control participant, has undergone breast implant surgery with silicone gel-filled breast implants

结局指标

主要结局

Long-term safety of Sientra Silicone Gel Breast Implants in women

时间窗: 10-years

次要结局

未报告次要终点

研究者

发起方
Sientra, Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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