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eural control of knee laxity in functional tasks after an ACL reconstructio

Conditions
Anterior cruciate ligament reconstruction
knee ligament surgery
10043237
Registration Number
NL-OMON46731
Lead Sponsor
Bewegingswetenschappen
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
40
Inclusion Criteria

Patients after an anterior cruciate ligament reconstruction using an autograft hamstring tendon
Patients between 18-45 years of age
Patients between 12 and 24 months after surgery

Exclusion Criteria

Serious cartilage damage of the lower extremity
Revision anterior cruciate ligament reconstruction
Osteotomy of the tibia or femur
Contralateral anterior cruciate ligament reconstruction
Other self-reported orthopedic or neurologic disorders that impair lower limb function.

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The main study parameters will be:<br /><br>- The passive and active anterior tibia translation.<br /><br>- Muscle activity of the lateral and medial hamstrings, lateral and medial<br /><br>gastrocnemius, rectus femoris, medial and lateral vasti.<br /><br>- The slope of the tibia plateau. </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>The secondary study parameters will be:<br /><br>- Sagittal knee angles<br /><br>- Sagittal knee moments<br /><br>- Ground reaction forces<br /><br>- The Beighton score, a scoring system for joint laxity and hypermobility </p><br>
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