CTRI/2022/11/047427
Completed
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
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: O- Medical and Surgical
- Sponsor
- Healthium Medtech Limited
- Enrollment
- 54
- Status
- Completed
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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).
Exclusion Criteria
- •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.
Outcomes
Primary Outcomes
Not specified
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