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ACL Reconstruction With/Without ALL Reconstruction

Prospective, Randomized, Double Blinded Trial Comparing Clinical, Radiological and Laboratory Outcomes of Anterior Cruciate Ligament Reconstruction With or Without Concomitant AnteroLateral Ligament Reconstruction.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05461625
Enrollment
762
Registered
2022-07-18
Start date
2021-09-01
Completion date
2024-12-01
Last updated
2022-07-18

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

Conditions

ACL Injury, ALL

Keywords

ACL, ALL

Brief summary

This study will compare Anterior Cruciate Reconstruction with or without Anterolateral Ligament Reconstruction in patients with ACL injury. The purpose of this study is evaluate if addition of ALLr to ACLr provides better clinical, radiological and laboratory outcomes.

Detailed description

This study compare ACL reconstruction and additional tenodesis or ALL recontruction described by Arnold. Patients will be randomized fot this tree group and surgeon will be blinded. Anterolateral ligament reconstruction could play a role in augmenting rotational stability in the ACL-reconstructed knee and are most likely to benefit hyperlax patients, revision cases, pivoting athletes, and those with IKDC grade III pivot shifts. In our study we will would like to confirm this hypothesis.

Interventions

PROCEDUREACL reconstruction

Anterior cruciate ligament reconstruction

OTHERALL anatomic

anatomic anterolateral ligament reconstruction

OTHERALL tenodesis

anterolateral ligament teondesis

Sponsors

Centre of Postgraduate Medical Education
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

\- primary ACL injury

Exclusion criteria

* no informed consent to participate in the study * age under 18 years or above 65 * multilligament injury or single plane knee instability (medial, lateral) * another musculoskeletal disorders in lower limb * lower limb deformity requiring axis correction below 4o or above 12.5o * joints inflammatory diseases * ASA score \> II

Design outcomes

Primary

MeasureTime frameDescription
Knee stability24 monthsKT-1000 assesment for knee stability

Secondary

MeasureTime frameDescription
KOOS (Knee injury and Osteoarthritis Outcome Score)6 weeksKnee Injury and Osteoarthritis Outcome Score; KOOS is intended to be used for knee injury that can result in post traumatic osteoarthritis (OA); KOOS has high test-retest reliability. In patients with knee injury, ICCs for the Pain subscale range from 0.85-0.93, the Symptoms subscale from 0.83-0.95, the ADL subscale from 0.75-0.91, the Sport/Rec subscale from 0.61-0.89 and the QOL subscale from 0.83-0.95. In patients with knee OA, ICCs for the Pain subscale range from 0.8-0.97, the Symptoms subscale from 0.74-0.94, the ADL subscale from 0.84-0.94, the Sport/Rec subscale from 0.65-0.92 and the QOL subscale from 0.6-0.91 (4).
Tegner Lysholm Knee Scoring Scale6 weeksThe Lysholm Knee Scoring Scale is a patient-reported instrument that consists of subscales for pain, instability, locking, swelling, limp, stair climbing, squatting, and the need for support. Scores range from 0 (worse disability) to 100 (less disability).
IKDC (International Knee Documentation Committee) subjective knee evaluation6 weeksIKDC is subjective scale that provides patients with an overall function score. Total to a scaled number ranges from 0 to 100. highr number representing higher levels of function.
Functional tests12 monthshop-for-distance
VAS (Visual analog scale)6 weeksThe pain VAS is a unidimensional measure of pain intensity. The most simple VAS is a straight horizontal line of fixed length, usually 100 mm. The ends are defined as the extreme limits of the parameter to be measured (symptom, pain, health)\[8\] orientated from the left (worst) to the right (best).
KOOS PF (Knee injury and Osteoarthritis Outcome Score Patellofemoral)6 weeksthe 'Knee Injury and Osteoarthritis Outcome Score Patellofemoral' questionnaire (KOOS-PF) is frequently used to measure symptoms and function among the people with PFJ-OA. This scale is scored from 0 to 100, with 100 representing no disability and 0 representing maximum disability
SF-36 (36-Item Short Form Survey)6 weeksQuality of life

Countries

Poland

Contacts

Primary ContactRafal Kaminski
rkamiski@spskgruca.pl+48227794031

Outcome results

None listed

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