NL-OMON54833已完成不适用
A Prospective Multicenter Longitudinal Cohort Study of the mymobility Platform - mymobility clinical study
Zimmer Biomet Nederland bv0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •Subject must be 18 years of age or older.
- •Subject is indicated for a primary, unilateral total or partial knee
- •arthroplasty, or total hip arthroplasty based on a physical exam.
- •Investigator plans to treat subject with a Zimmer Biomet device as part of
- •their clinical care.
- •Subject must own and maintain an iPhone 6 or newer (excluding the iPhone SE).
- •Subject is mobile with no more than a single cane/single crutch assist.
排除标准
- •Subject is a current alcohol or drug abuser. • Subject has inflammatory
- •arthropathies which would interfere or compromise the activity profiles within
- •this study. • Subject is considered a member of a protected population (e.g.,
- •prisoner, mentally incompetent, etc.). • Subject is currently participating in
- •any other surgical intervention, physical therapy or pain management study
- •which would compromise the results of this study. • Subject requires
- •simultaneous or staged bilateral replacements, staged <90 days apart.
- •Subjects can be enrolled into the study for the second, staged arthroplasty if
- •scheduled >89 days after their first, contralateral replacement.
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