EUCTR2013-000949-39-PL进行中（未招募）不适用
An Observational Study Providing 12 Months of Safety Follow-Up from First Exposure to HP802-247 in Subjects Who Participated in Study 802-247-09-032(EU)
Smith & Nephew Inc.0 个研究点目标入组 440 人开始时间: 2013年8月14日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 440
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •- The informed consent document must be read, signed, and dated by the subject or the subject’s legally authorized representative before conducting any study procedures or exams. A photocopy of the signed informed consent document must be provided to the subject, and the original signed document placed in the subject’s chart.
- •- Subject was randomized in 802-247-09-032 and received at least one application of test article.
- •- Subject has ended their participation in 802-247-09-032 by virtue of completing the study, or by dropping out prior to completion.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 264
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 176
排除标准
- •Subjects who refuse to provide written informed consent for this study will be excluded from this study.
研究者
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