CTRI/2022/11/047339
Completed
Phase 4
A retrospective observational study on functional outcomes following arthroscopic Anterior Cruciate Ligament (ACL) reconstruction using loop suture button and/or interference screw of SIRONIX
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Health Condition 1: O- Medical and Surgical
- Sponsor
- Healthium Medtech Limited
- Enrollment
- 33
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Male and female patients aged between 18 to 60 years at the time of surgery
- •2\. Patients who underwent ACL reconstruction using loop suture button and/or HELYSIS interference screw of SIRONIX between April 2018 to July 2022
- •3\. Patients who have provided verbal consent or written informed consent (if subject visits the site) to participate in the study
Exclusion Criteria
- •1\. Unable to provide verbal consent or written informed consent and unwilling to be followed up telephonically
- •2\. Patients who have suffered traumatic injury after surgery affecting the operated knee
- •3\. Patients who are unable to move/walk due to critical illness other than operated knee complications
Outcomes
Primary Outcomes
Not specified
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