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NCT Number: NCT03073083

Graft Selection in Anatomic Anterior Cruciate Ligament Reconstruction

A rupture of the anterior cruciate ligament (ACL) is a severe injury of the knee. The current gold Standard treatment for young and active patients with instability, is a surgical ACL reconstruction. However, there still is no consensus on which graft is best suited for this.The aim of the current multi-center randomized controlled trial was to investigate the hypothesis that an anatomic single bundle anterior cruciate ligament reconstruction with a (flat) quadriceps tendon autograft is at least as effective as reconstruction of the ruptured anterior cruciate ligament with a patella tendon autograft or a hamstringtendon autograft, in terms of failure, measured 2 years postoperatively. Failure is defined gedefinieerd as pathologicai laxity, complaints of knee instability in the absence of any pathological laxity and/or discontinuïty ofthe graft on MRl or arthroscopy.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Martini Hospital Groningen, Groningen, Netherlands

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About this study

A rupture of the anterior cruciate ligament (ACL) is a severe injury of the knee. The current gold Standard treatment for young and active patients with instability, is a surgical ACL reconstruction. However, there still is no consensus on which graft is best suited for this.

Paradigms on the different types of auto grafts and their weaknesses and benefits originate mostly from the eighties and nineties, when the patella tendon was being replaced by the hamstring graft as the 'new' gold standerd. Nowadays, the philosophy of isometrie tunnel placement has been abandoned, and has been replaced by the philosophy of anatomie reconstructions. The question then arises: Are the results of the comparative studies, and the current paradigms, still applicable, now that the philosophy has transitioned from isometric to anatomic tunnel placement? Irrespective of the disadvantages compared to the patellatendon autograft, such as a higher re-rupture and revision percentage when used in patients under 25 years old, the hamstring autograft is currently the most used graft for ACL reconstruction worldwide. The question then arises: is it justified that the hamstringgraft is the most used graft worldwide? Rehabilitation protocols are often not, or poorly, described, despite it's significant effect on the outcome and co morbidity of an ACL reconstruction. Especially anterior knee pain, which is often mentioned as a disadvantage of the patellagraft, is significantly influenced by rehabilitation protocols. The introduction and implementation of a nation-wide evidence-based rehabilitation protocol in The Netherlands created uniformity of rehabilitation treatment, and the possibility to generalize scientific conclusions. The question then arises: Due to new insights in rehabilitation and implementation of new protocols, is the anterior knee pain, the often mentioned disadvantage ofthe patelia tendon graft, stiil a relevant disadvantage? The quadriceps tendon autograft is a less often used graft. Nevertheless, research has shown that it seems like a good alternative for the patella tendon and hamstring autograft. Functional outcome is similar, while less donorsite morbidity is reported compared to the patellatendon and hamstring autograft. The question then arises: Is it fair that the quadriceps tendon is rarely used as an autograft for ACL reconstruction? Increasing knowledge of the anatomy of the ACL results in new insights in the methods to achieve true anatomie ACL reconstruction. New arguments support the use of the patella tendon - and even the quadriceps tendon - over the use of the hamstringgraft, because their anatomic similarities to the anterior cruciate ligament might be better suited to restore knee kinematics. The question then arises: are the flat-shaped patella tendon autograft and quadriceps tendon autograft better suited to restore the anatomy of the ruptured ACL than the round hamstring graft? Hypothesis Tlie hypothesis is that anatomic reconstruction ofthe ruptured anterior cruciate ligament with a (flat) quadriceps tendon autograft is at least as effective as reconstruction of the ruptured anterior cruciate ligament with a patella tendon autograft or a hamstring tendon autograft, in terms of failure, measured 2 years postoperatively. Failure is defined as pathological laxity, complaints of knee instability in the absence of any pathological laxity and/or discontinuïty of the graft on MRl or arthroscopy.

Objective of the study:

Primary objective:

To investigate the hypothesis that an anatomic single bundle anterior cruciate ligament reconstruction with a (flat) quadriceps tendon autograft is at least as effective as reconstruction of the ruptured anterior cruciate ligament with a patella tendon autograft or a hamstring tendon autograft, in terms of failure, measured 2 years postoperatively. Failure is defined gedefinieerd as pathologicai laxity, complaints of knee instability in the absence of any pathological laxity and/or discontinuïty of the graft on MRl or arthroscopy.

**Graft failure at 2 years (originally registered). Due to premature termination, this outcome was underpowered and analyzed exploratorily. The IKDC Subjective Knee Form score was analyzed as the main outcome in the final report.**

Secondary objectives:

patiënt reported outcome measures (PROMs), clinimetrics, radiological assessment, duration of rehabilitation necessary for return to sports and daily activities and the level of sport activities to which the patiënt returned, in patients treated with an anterior cruciate ligament reconstruction using a patellatendon autograft, hamstringtendon autograft of quadricepstendon autograft, as measured in the short-term (6 weeks, 6,9,12 months postoperatively), mid-term (2 years postoperatively) and long-term (5 and 10 years postoperatively).

Study design:

Multicenter blocked stratified randomised controlled trial with varying block sizes (n=3, 6, 9, 12). Patients with an anterior cruciate ligament rupture, confirmed by an orthopaedie surgeon (as evident from anamnesis, physical examination and radiographic imaging) who meet the inclusion criteria and do not have any of the exclusion criteria, will be asked to partieipate in this study.

Baseline measurements will be performed, after informed consent is obtained. Allocation of treatment of the included patients will be performed in the operating room (OR), where patients will be randomised (blocked and stratified) per clinic, to have ACL reconstruction with a patella tendon autograft, hamstring tendon autograft or quadriceps tendon autograft. Stratification will be based on age (18-25 and >25), level of sport activities (Tegner Activity Level Scale 5-7 and 8-10) and surgeon.

Follow-up identical to the follow-up of standard care, with standard checkups after 6 weeks, 6, 9, months and 1 and 2 years. Two extra follow-up moments (after 5 and 10 years) will be planned.

** Study inclusion stopped early due to slower-than-expected recruitment (patient preference, COVID-19) and changes in standard care including the addition of a Lemaire procedure. Continuing without it was no longer appropriate. The achieved sample size allowed adequate power (80%) for non-inferiority analysis of the IKDC subjective score (-10 points difference, n = 23 per group). Follow-up of enrolled participants continues.**

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients active in sports, Tegner =/>5
  • Primary ACL rupture, evident from anamnesis (acute trauma, snapping sensation, swelling within several hours, feeling of instability), physical examination (positive Lachman test, anterior drawertest and/or pivot shift test), radiograph and MRl
  • Willing to comply to the suggested (nationwide standard) rehabilitation protocol, supen/ised by a NFVS registerd sport-physical therapist
  • <6 months between initial trauma and surgery

Exclusion criteria

  • History of knee surgery on the same side
  • History of tendon removal on the same side
  • Accompanying ligament injury ofthe knee, evident from anamnesis, physical examination, radiograph and MRl, defined as an ACL rupture in combination with a posterior cruciate ligament or collateral ligament injury,
  • Peroperative discovery of cartilage damage; larger than 2cm2 and more than 50% depth
  • Peroperative discovery of meniscus injury witch requires a meniscectomy of more than 20% or meniscus sutures
  • Osteoarthritis of Kellgren and Lawrence grade 2 or more, as evident from the radiograph
  • Severe malalignment of the leg
  • Tendency to form excessive scar tissue, such as arthrofibrosis
  • Muscular, neurological or vascular anomalies that influence healingtime or rehabilitation
  • Infection
  • Known hypersensitivity to any of the used materials
  • Long term relevant medication use such as prednisolone or cytostatics
  • Pregnancy at the time of inclusion or surgery
  • Known osteoporosis

Treatment and study plan

Hamstring tendon autograft

Procedure

ACL reconstruction surgery with hamstring tendon

Other names: all-inside AMPS technique Arthrex

Pattella tendon autograft

Procedure

ACL reconstruction surgery with patella tendon

Other names: Smith and Nephew

Quadriceps tendon autograft

Procedure

ACL reconstruction surgery with quadriceps tendon

Other names: all-inside AMPS technique Arthrex

Primary outcomes

  1. Physical examination ACL Failure

    Time frame: 2 years after ACL reconstruction surgery

    Presence / absence of anterior cruciate ligament failure. Failure is defined as pathologicai laxity, complaints of knee instability in the absence of any pathological laxity and/or discontinuïty ofthe graft on MRl or arthroscopy.

    Graft failure at 2 years (originally registered). Due to premature termination, this outcome was underpowered and analyzed exploratorily. The IKDC Subjective Knee Form score was analyzed as the main outcome in the final report. The IKDC subjective score was already powered at study design (-10 points non-inferiority margin; n = 23 per group, 80% power).

Secondary outcomes

  1. quality of life (ACL-QoL)

    Time frame: preoperative, 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery

    level of self-reported quality of life

  2. functional knee and health status (IKDC)

    Time frame: preoperative, 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery

    level of functional knee and current health status

  3. physical examination of knee (in)stability

    Time frame: preoperative, 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery

    instability in the absence of any pathological laxity and/or discontinuïty of the graft on MRl or arthroscopy.

  4. Knee and Injury Osetoarthritis Outcome Score questionnaire (KOOS)

    Time frame: preoperative, 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery

    self-reported level of physical activity in daily life

  5. sports intensity questionnaire (Tegner Activity Level)

    Time frame: preoperative, 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery

    self-reported level of pivoting sports execution

  6. questionnaire

    Time frame: preoperative, 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery

    level of physical activity (Lysholm score)

  7. knee pain

    Time frame: preoperative, 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery

    self-reported level of pain during activity and rest on visual analogue scale

  8. Instability knee

    Time frame: preoperative, 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery

    VAS score (patient perception)

  9. satisfaction with result of ACL surgery

    Time frame: 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery

    self-reported level of satisfaction with ACL surgery on visual analogue scale

  10. physical examination

    Time frame: 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery

    degree of knee (in)stability during jumping tests (Leg Symmetry Index)

  11. physical examination

    Time frame: preoperative, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery

    degree of knee (in)stability in strenght (Leg Symmetry Index)

  12. Lachman test

    Time frame: 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery

    physical examination: degree of knee (in)stability measured by rollimeter (operated-nonoperated side ratio)

  13. Degree of Osteoarthritis on x-ray

    Time frame: Baseline, 1,2,5 10 years after ACL reconstruction surgery

    Kellgren-Lawrence classification will be applied to assess the degree of osteoarthritis

Other outcomes

  1. Knee instability during jumping movements

    Time frame: 1 and 2 years after ACL reconstruction surgery

    Measured during jumping test. At OCON patients will be equiped with 3D accelerometer sensors in order to quantify the degree of (in)stability of the affected knee during the execution of jump tests under the supervision of a specialized sports physiotherapist

  2. Complications and other adverse events

    Time frame: 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery

    number and type complications and adverse events

Sponsors and collaborators

Lead sponsor

Orthopedisch Centrum Oost Nederland

Other

Collaborators

  • Gelderse Vallei Hospital
  • Martini Hospital Groningen

Registry information

Official study title

Graft Selection in Anatomic Anterior Cruciate Ligament Reconstruction: Patella, Hamstrings or Quadriceps Tendon Autograft

Acronym: Grafttype

Important dates

Study start
2017
Primary completion
2031
Study completion
2031
First posted
Mar 8, 2017
Registry last updated
Nov 25, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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