Sprains and strains involving the cruciate ligament (anterior or posterior) of the knee
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Volunteers of both sexes; minimum age of 18 years and maximum age of 45 years; undergoing reconstruction of the anterior cruciate ligament and extra-articular reinforcement of the anterior oblique ligament with a graft from the long peroneal tendon
Exclusion criteria
Exclusion criteria: Volunteers with previous surgeries on the operated knee; with chondral lesions grades III or IV of the Outerbridge classification for chondral lesions; with other associated ligament injuries in the same knee; who did not complete the minimum follow-up of 24 months; who suffered new traumatic injuries in the operated knee during the follow-up period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1: we expect to obtain the Lysholm and IKDC (International Knee Documentation Committee) scores preoperatively and at 24 months; evaluate the Lachman test (grading from 0 to 3+); evaluate the pivot-shift test (grading from 0 to 3+); evaluate postoperative complications; evaluate the rate of return to sports; check the patient's satisfaction level (scale from 0 to 10); symptoms in the graft donor area (foot and ankle); evaluate the AOFAS (American Orthopaedic Foot and Ankle Society) and FADI (Foot and Ankle Disability Index) scores preoperatively and at 24 months;Outcome found 1: Mean Lysholm score improved from 71.5 ± 11.2 to 98.5 ± 2.0 (? +27.0, p < 0.001), and IKDC from 73.0 ± 10.1 to 98.5 ± 1.9 (? +25.6, p < 0.001). VAS (Analog Visual Scale) pain decreased from 5.93 ± 2.89 to 0.43 ± 0.62 (? -5.51, p < 0.001). AOFAS (American Orthopaedic Foot and Ankle Society) scores remained stable (99.4 ± 2.0 pre- and postoperatively), while FADI (Foot and Ankle Disability Index) showed no clinically significant change (99.1 ± 4.0 to 98.6 ± 4.2). No major complications or clinically relevant donor-site morbidity were observed. Return-to-sport rate data were not available. Mean patient satisfaction score was high across the cohort | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes are expected | — |
Countries
Brazil
Contacts
Irmandade Santa Casa de Misericórida de São Paulo