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Clinical Trials/CTRI/2022/12/048062
CTRI/2022/12/048062
Completed
未知

A Retrospective, Observational, Study to Evaluate the Functional Outcomes in Patients Who Underwent Arthroscopic Rotator Cuff Tears Repair Using Sironix Suture Anchor

Healthium Medtech Limited0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: O- Medical and Surgical
Sponsor
Healthium Medtech Limited
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Male/ Female Patients of 18 to 80 years of age.
  • 2\. Patients who underwent arthroscopic rotator cuff tears repair using Sironix suture anchor between the period of January 2019 to June 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 traumatic injury to the same shoulder post rotator cuff tears repair procedure.

Outcomes

Primary Outcomes

Not specified

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