- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06341192
Comparison Between Combined ALLR With Single Bundle and Double Bundle Anterior Cruciate Ligament Reconstruction (ALLR)
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
Status
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Cheng-Pang Dr. Yang
- Phone Number: 886-3-3281200 ext. 2163
- Email: ronnie80097@gmail.com
Study Locations
-
-
taoyuan
-
Taoyuan District, taoyuan, Taiwan, 333
- Recruiting
- Chang Gung Memorial Hospital
-
Contact:
- Cheng-Pang Yang, Dr
- Email: ronnie80097@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
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
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
Sponsor
Investigators
- Principal Investigator: Cheng-Pang Dr. Yang, Cheng Gung Memorial Hospital
Publications and helpful links
General Publications
- Sonnery-Cottet B, Thaunat M, Freychet B, Pupim BH, Murphy CG, Claes S. Outcome of a Combined Anterior Cruciate Ligament and Anterolateral Ligament Reconstruction Technique With a Minimum 2-Year Follow-up. Am J Sports Med. 2015 Jul;43(7):1598-605. doi: 10.1177/0363546515571571. Epub 2015 Mar 4.
- Cameron KL, Peck KY, Davi SM, Owens CRBD, Svoboda CRSJ, DiStefano LJ, Marshall SW, de la Motte SJ, Beutler CRAI, Padua DA. Association Between Landing Error Scoring System (LESS) Items and the Incidence Rate of Lower Extremity Stress Fracture. Orthop J Sports Med. 2022 Jun 9;10(6):23259671221100790. doi: 10.1177/23259671221100790. eCollection 2022 Jun.
- Helito CP, Helito PVP, Costa HP, Demange MK, Bordalo-Rodrigues M. Assessment of the Anterolateral Ligament of the Knee by Magnetic Resonance Imaging in Acute Injuries of the Anterior Cruciate Ligament. Arthroscopy. 2017 Jan;33(1):140-146. doi: 10.1016/j.arthro.2016.05.009. Epub 2016 Jun 17.
- Batty LM, Firth A, Moatshe G, Bryant DM, Heard M, McCormack RG, Rezansoff A, Peterson DC, Bardana D, MacDonald PB, Verdonk PCM, Spalding T, Getgood AMJ; STABILITY Study Group; Willits K, Birmingham T, Hewison C, Wanlin S, Firth A, Pinto R, Martindale A, O'Neill L, Jennings M, Daniluk M, Boyer D, Zomar M, Moon K, Pritchett R, Payne K, Fan B, Mohan B, Buchko GM, Hiemstra LA, Kerslake S, Tynedal J, Stranges G, Mcrae S, Gullett L, Brown H, Legary A, Longo A, Christian M, Ferguson C, Mohtadi N, Barber R, Chan D, Campbell C, Garven A, Pulsifer K, Mayer M, Simunovic N, Duong A, Robinson D, Levy D, Skelly M, Shanmugaraj A, Howells F, Tough M, Thompson P, Metcalfe A, Asplin L, Dube A, Clarkson L, Brown J, Bolsover A, Bradshaw C, Belgrove L, Millan F, Turner S, Verdugo S, Lowe J, Dunne D, McGowan K, Suddens CM, Declercq G, Vuylsteke K, Van Haver M. Association of Ligamentous Laxity, Male Sex, Chronicity, Meniscal Injury, and Posterior Tibial Slope With a High-Grade Preoperative Pivot Shift: A Post Hoc Analysis of the STABILITY Study. Orthop J Sports Med. 2021 Apr 6;9(4):23259671211000038. doi: 10.1177/23259671211000038. eCollection 2021 Apr.
- Sonnery-Cottet B, Daggett M, Fayard JM, Ferretti A, Helito CP, Lind M, Monaco E, de Padua VBC, Thaunat M, Wilson A, Zaffagnini S, Zijl J, Claes S. Anterolateral Ligament Expert Group consensus paper on the management of internal rotation and instability of the anterior cruciate ligament - deficient knee. J Orthop Traumatol. 2017 Jun;18(2):91-106. doi: 10.1007/s10195-017-0449-8.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- ChangGungMH ALL SB DB
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
- 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.
- 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
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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