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Clinical Trial Summary

The aim is to determine the sensitivity and specificity of a screening tool to identify patients who undergo ACL reconstruction (non-copers) after 3 months of standard rehabilitation following an anterior Cruciate ligament (ACL) injury.


Clinical Trial Description

All included patients are referred to municipal rehabilitation to resolve effusion and range of motion deficits before the first screening (baseline screening) is completed. Hereafter the patients follow 3 months municipal rehabilitation before the second screening (3 months screening). A physiotherapist performs the screening and at the second screening, this is performed prior to consulting an orthopaedic surgeon. ;


Study Design


Related Conditions & MeSH terms

  • Anterior Cruciate Ligament Injuries

NCT number NCT04847258
Study type Observational
Source Vejle Hospital
Contact Kamilla Arp, MSc
Phone +45 79406796
Email kamilla.dessau.arp@rsyd.dk
Status Recruiting
Phase
Start date March 19, 2021
Completion date May 31, 2024

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