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Clinical Trials/CTRI/2022/11/047290
CTRI/2022/11/047290
Completed
N/A

Evaluation of the Functional Outcomes in Patients Who Underwent Arthroscopic Anterior Cruciate Ligament (ACL) Reconstruction Procedure Using Sironix Suture Button and/or Sironix Interference Screw: A Retrospective, Observational, Multicentric study

Healthium Medtech Limited0 sites113 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
Health Condition 1: O- Medical and Surgical
Sponsor
Healthium Medtech Limited
Enrollment
113
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Male/ Female Patients of 18 to 60 years of age.
  • 2\. Patients who underwent Arthroscopic Anterior Cruciate Ligament (ACL) Reconstruction Procedure Using Sironix Suture Button and/or Sironix Interference Screw between the period of April 2018 to July 2022
  • 3\. Patient willing to give written informed consent to participate in the study when attending an in\-clinic follow\-up visit, or providing verbal consent during the telephonic follow\-up visit.

Exclusion Criteria

  • 1\. Patients not responding to calls after three attempts or not interested to participate in the study.
  • 2\. Patients with injury or re\-surgery to the same knee post ACL reconstruction procedure.

Outcomes

Primary Outcomes

Not specified

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