CTRI/2022/11/047427已完成未知
A Single-center, Non-interventional, Observational study to assess Clinical Outcomes and Patient Reported Outcomes after treatment of Rotator Cuff Tears using Sironix Suture Anchor Devices
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 54
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 surgery with Sironix Suture Anchor Devices with a minimum of 6 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 are diagnosed with other serious shoulder injury that can cause shoulder pain (tumor of shoulder, acute fracture, and dislocation of shoulder).
- •2. Patients who are not willing to attend the follow-up.
研究者
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