ong term Follow-Up after ACL reconstructio

Completed

• Conditions: ACL tear; anterior cruciate ligament rupture; 10043237

• Registration Number: NL-OMON42229
• Lead Sponsor: Medisch Centrum Alkmaar

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 100

Inclusion Criteria

In order to be eligible to participate in this study, a subject must meet all of the following criteria:;• Unilateral ACL rupture;
• Suitable to one of the subgroups;
• Can be contacted;
• Are willing and able to participate in the study protocol and follow-up visitation of the outpatient clinic

Exclusion Criteria

Subjects will be excluded when they:;• are not willing to participate;
• are not capable of participating (either mentally or physically);
• have deceased;
• are unable to undergo radiography (e.g. due to pregnancy).

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Radiographic outcome measures<br /><br>• Evidence of osteoarthritis based on Kellgren-Lawrence scale<br /><br>Clinical outcome measures<br /><br>• Range of Motion<br /><br>• Knee stability</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>• Quality of Life<br /><br>• Pain<br /><br>• Status of return to work and daily activities<br /><br>• Secondary surgical procedures<br /><br>• Surgical complication<br /><br>• Patient characteristics</p><br>