Comparison Between Combined ALLR With Single Bundle and Double Bundle Anterior Cruciate Ligament Reconstruction (ALLR)

September 24, 2025 updated by: Chang Gung Memorial Hospital

Clinical Comparison and Motion Analysis of Sports Function Between Combined Anterolateral Ligament Reconstruction With Single Bundle and Double Bundle Anterior Cruciate Ligament Reconstruction

The goal of this clinical trial is to test and compare different surgical techniques in patients with anterior cruciate ligament (ACL) injuries. The main questions it aims to answer are:

  • What are the optimal criteria for selecting between single-bundle ACL reconstruction combined with anterolateral ligament (ALL) reconstruction versus double-bundle ACL reconstruction combined with ALL reconstruction?
  • How do these two surgical techniques compare in terms of post-operative knee stability, functional outcomes, and reducing re-tear rates?

Participants will:

  • Undergo pre-operative MRI imaging, ligament stability testing, and motion analysis evaluations
  • Be randomly assigned to either:

    • Single-bundle ACL + ALL reconstruction
    • Double-bundle ACL + ALL reconstruction
  • Receive the assigned surgical procedure
  • Participate in post-operative follow-ups, ligament stability testing, and motion analysis at 6 months and 1 year

Researchers will compare the single-bundle ACL + ALL group and the double-bundle ACL + ALL group to see if one technique demonstrates superior knee stability, functional outcomes (e.g. return to sport ability), and lower ACL re-tear rates.

Study Overview

Detailed Description

Anterolateral ligament(ALL) combined with anterior cruciate ligament reconstruction(ACL) has become more and more popular in recent years, as ALL could protect the ACL graft in tibial internal rotation, and prevent the ACL graft from rupture. Cottet et al. proposed a minimal invasive method with Y-figure construct of ALL, without acquiring additional graft from the patient. Their data showed significant lower graft re-rupture rate and faster return-to-sport(RTS). There are many different techniques of ACL combined ALL reconstruction. While these methods mostly are single bundle ACL combined ALL reconstruction. Previous cadaver studies told that the anterior cruciate ligament is composed of anteromedial and posterolateral bundle. It had been debated between single bundle and double bundle ACL reconstruction for years. As a result, it is meaningful to compare the clinical outcomes between ALL combined with single bundle or double bundle ACL reconstruction. Our studies included MRI image, arthrometer measurement and optical motion capture system. We hope to compare the clinical outcomes and sports function between A: single bundle ACL combined ALL reconstruction and B: double bundle ACL combined ALL reconstruction.

Study Type

Interventional

Enrollment (Estimated)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • taoyuan
      • Taoyuan District, taoyuan, Taiwan, 333

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Patients plan to receive ACL surgery
  • at least 18 years old

Exclusion Criteria:

  • Presented history of the injured leg or congenital abnormality

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Double bundle ACL combined anterolateral ligament reconstruction
ACL reconstruction with triple folded semitendinosus and non folded gracilis and fibertape

Double-Bundle ACL + ALL Reconstruction Group:

Patients in this group will undergo anatomic double-bundle ACL reconstruction using two graft bundles to more anatomically replicate the native ACL's anteromedial and posterolateral bundles.

Like the single-bundle group, they will also have supplemental ALL reconstruction performed using a portion of the graft material.

The double-bundle ACL reconstruction aims to better restore the ACL's complex anatomic footprint and bundles' tension patterns.

Experimental: Single bundle ACL combined anterolateral ligament reconstruction

Single-Bundle ACL + ALL Reconstruction Group:

Patients in this group will undergo reconstruction of the anterior cruciate ligament (ACL) using a single-bundle graft technique.

In addition, they will have the anterolateral ligament (ALL) reconstructed using a portion of the same graft material.

The single ACL bundle is typically positioned to replicate the anatomic footprint of the native ACL.

For the ALL reconstruction, a commonly used technique is the Sonnery-Cottet ALL reconstruction using a gracilis tendon graft.

This combines an intra-articular ACL reconstruction with an extra-articular lateral tenodesis to improve rotational instability.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Knee ligament stability:
Time Frame: Preoperative, 6 months, 1 year
Anterior tibial translation measured using a ligament arthrometer (GNRB) to objectively quantify anteroposterior knee laxity
Preoperative, 6 months, 1 year
Knee ligament stability clinical evaluation
Time Frame: Preoperative, 6 months, 1 year
Lachman test
Preoperative, 6 months, 1 year
Knee ligament stability clinical evaluation
Time Frame: Preoperative, 6 months, 1 year
pivot shift test
Preoperative, 6 months, 1 year
Knee ligament stability clinical evaluation
Time Frame: Preoperative, 6 months, 1 year
Anterior drawer test
Preoperative, 6 months, 1 year
Functional performance and return to sport
Time Frame: Preoperative, 6 months, 1 year
Lower limb muscle strength
Preoperative, 6 months, 1 year
Functional performance and return to sport
Time Frame: Preoperative, 6 months, 1 year
Lower limb symmetry index
Preoperative, 6 months, 1 year
Patient-reported outcome measures (PROMs)
Time Frame: Preoperative, 3 months, 6 months, 9 months, 1 year
International Knee Documentation Committee (IKDC) subjective score. The IKDC is a patient-completed tool, which contains sections on knee symptoms (7 items), function (2 items), and sports activities (2 items). Scores range from 0 points (lowest level of function or highest level of symptoms) to 100 points (highest level of function and lowest level of symptoms).
Preoperative, 3 months, 6 months, 9 months, 1 year
Patient-reported outcome measures (PROMs)
Time Frame: Preoperative, 3 months, 6 months, 9 months, 1 year
Marx's activity score;The Marx Scale consists of four questions concerning four activities or actions: running, cutting, deceleration, and pivoting. The patient or survey respondent is asked to report on the frequency with which they performed the activity in their healthiest state within the past year. From 0 point(the worst) to 16 points(the best).
Preoperative, 3 months, 6 months, 9 months, 1 year
Patient-reported outcome measures (PROMs)
Time Frame: Preoperative, 3 months, 6 months, 9 months, 1 year
SANE score, The Single Assessment Numeric Evaluation (SANE) is a patient rating from 0-100. Patients rate their current illness score in relation to their pre-injury baseline
Preoperative, 3 months, 6 months, 9 months, 1 year
Imaging
Time Frame: Preoperative, 1 year
Pre- and post-operative X-ray analysis to assess bone tunnels position
Preoperative, 1 year
Imaging
Time Frame: Preoperative, 1 year
Pre- and post-operative MRI analysis to assess graft ligamentization.
Preoperative, 1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Cheng-Pang Dr. Yang, Cheng Gung Memorial Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 26, 2024

Primary Completion (Estimated)

August 31, 2026

Study Completion (Estimated)

October 31, 2026

Study Registration Dates

First Submitted

March 18, 2024

First Submitted That Met QC Criteria

March 25, 2024

First Posted (Actual)

April 2, 2024

Study Record Updates

Last Update Posted (Estimated)

September 25, 2025

Last Update Submitted That Met QC Criteria

September 24, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

  1. Protection of participant privacy and confidentiality is paramount in this study involving sensitive medical data and procedures. Sharing identifiable IPD could breach the trust and privacy of these patients undergoing knee surgeries.
  2. The informed consent process likely did not explicitly state or obtain approval from participants to share their individual-level data, including medical images, functional assessments, and clinical outcomes, with third parties outside the research team.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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