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Evaluation of the Results of Two Different Methods in Management of Antero-lateral Instability of the Knee

Evaluation of the Results of Two Different Methods in Management of Antero-lateral Instability of the Knee

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06222814
Enrollment
40
Registered
2024-01-25
Start date
2023-09-01
Completion date
2025-08-31
Last updated
2024-01-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anterior Cruciate Ligament Injuries

Brief summary

This randomized clinical study will be conducted to compare the results of anterior cruciate ligament reconstruction (ACLR) combined with either anterolateral ligament reconstruction using peroneus longus autograft or extra-articular tenodesis (Modified Lemaire) in management of antero-lateral instability of the knee

Detailed description

Patients will undergo an anatomic ACLR in a standardized fashion by the same team of surgeons. They are randomly divided into 2 groups either ACLR plus ALL reconstruction or ACLR combined with LET in a 1:1 ratio. There are multiple graft options for ACL-R, but here for the study, the hamstring autograft is harvested following the traditional technique. The graft is measured and bony tunnels are drilled. An anatomical reconstruction technique is used in all cases. In group A: the surgeon will harvest peroneus longus graft, then sutured to the double bundle hamstring graft. The graft diameters are measured and recorded. The graft is pulled through the femoral tunnel and passed through the tibial tunnel. The single portion of the graft is passed freely through the tibial and femoral tunnels until the quintuple graft portion occupies both tunnels. The graft is then pulled, and an interference screw (Smith & Nephew Endoscopy) is fixed to the femur. The next step is to fix the inferior end of the quintuple graft to the tibia after pre-tensioning. After tibial fixation, the remaining PL is passed through the subcutaneous and ALL tunnels. The ligament is fixed under traction, mild valgus stress, and 30' of flexion 1.5 cm from the joint line into a midpoint between Gerdy's tubercle and the fibular head. In group B: the surgeon will use a triple STG hamstring (6- strands) tendon graft. The graft diameters are measured and recorded. Then, LET is performed in a standardized fashion as described in the modified Lemaire technique. LET is fixed with interference screws (Smith & Nephew Endoscopy). Femoral and tibial fixations are performed with bio-absorbable interference screws (Smith & Nephew Endoscopy).

Interventions

PROCEDUREACL reconstruction combined with anterolateral ligament reconstruction using peroneus longus autograft

ACL reconstruction combined with anterolateral ligament reconstruction using peroneus longus autograft

PROCEDUREACL reconstruction combined with extra-articular tenodesis (Modified Lemaire)

ACL reconstruction combined with extra-articular tenodesis (Modified Lemaire)

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

1. The ACL deficient knee was clinically manifested by physical examination and confirmed by MRI. 2. Age 18-45 years, skeletally mature patient. 3. A positive pivot shift test of at least grade II is required (significant anterolateral instability).

Exclusion criteria

1. Multiple ligament injuries or a polytraumatized patient 2. Revision cases. 3. Generalized laxity. 4. Symptomatic articular cartilage defect requiring treatment; Outerbridge \> grade II. 5. More than three degrees of varus or valgus malalignment

Design outcomes

Primary

MeasureTime frameDescription
Functional results of knee stability and return to normal activity12 months postoperativelyIKDC (International Knee Documentation Committee) subjective knee evaluation form

Countries

Egypt

Contacts

Primary ContactOmar Abdelkarim, Master
omar.ortho89@gmail.com01008016681
Backup ContactMohamed Ali, MD
mohamed.ali@yahoo.com01011954560

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026