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Clinical Trial Summary

The objective of the study is to assess re-rupture rates and patient outcomes from subjects with at least 5 year follow up, treated with the JewelACL device for ACL reconstruction. The impact of fixation type and autograft augmentation will also be assessed. All adverse events related to the JewelACL device will be recorded. This study is Sponsored by Xiros.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Anterior Cruciate Ligament Injuries

NCT number NCT04580290
Study type Observational
Source Xiros Ltd
Contact
Status Completed
Phase
Start date October 2, 2020
Completion date April 9, 2021

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