CTRI/2023/07/055329已完成Unknown
A Single-center, Non – interventional, Observational, Post market clinical follow-upstudy to assess Clinical Outcomes and Patient Reported Outcomes after treatment ofshoulder injuries using Sironix Suture Anchor Devices - NI
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 入组人数
- 60
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
入选标准
- •1)Male/female patients aged = 18 years and = 80 years at the time of surgery
- •2)Patients who had undergone treatment for either rotator cuff tear repair or bankart repair with Sironix suture anchor devices with a minimum of 4 months of follow-up
- •3)Patients who are willing to provide written informed consent (in case of a physical visit to the site) or verbal informed consent (in case of a telephonic visit)
排除标准
- •1)Patients who have had any traumatic injury to the operated shoulder post surgery.
- •2)Patients who are not willing to attend the follow-up.
研究者
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