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Anterior Cruciate Ligament InjuriesGrafttypeNCT03073083

Graft Selection in Anatomic Anterior Cruciate Ligament Reconstruction

A study testing Hamstring tendon autograft, Pattella tendon autograft and Quadriceps tendon autograft in people with Anterior Cruciate Ligament Injuries, run by Orthopedisch Centrum Oost Nederland at 2 sites in Netherlands.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Anterior Cruciate Ligament Injuries
What is being tested?
Hamstring tendon autograft, Pattella tendon autograft and Quadriceps tendon autograft
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
439 participants
Where
2 sitesNetherlands
Study dates
6 Mar 2017to Dec 2031
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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

Who cannot join

  • 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
Show all 14Show fewer
  • 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

Trial locations and contacts

2 sites in 1 country.

Netherlands2 sites
  • Martini Hospital Groningen

    Groningen, 9728 NT

  • OCON

    Hengelo

Other trials in Netherlands

About this study

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

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.

Read the detailed description

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.

Being tested
Hamstring tendon autograft, Pattella tendon autograft, Quadriceps tendon autograft
Keywords
autograft
Medical subject headings
Anterior Cruciate Ligament Injuries

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Hamstring tendon autograftProcedure or surgery

    Also called all-inside AMPS technique Arthrex

    ACL reconstruction surgery with hamstring tendon

  • Pattella tendon autograftProcedure or surgery

    Also called Smith and Nephew

    ACL reconstruction surgery with patella tendon

  • Quadriceps tendon autograftProcedure or surgery

    Also called all-inside AMPS technique Arthrex

    ACL reconstruction surgery with quadriceps tendon

Study groups in NCT03073083
Study groupRoleWhat they receive
Hamstring tendon autograftActive comparatorACL reconstruction surgery with hamstring tendon autograft
Receives: Procedure: Hamstring tendon autograft
Patella tendon autograftActive comparatorACL reconstruction surgery with pattella tendon autograft
Receives: Procedure: Pattella tendon autograft
Quadriceps tendon autograftActive comparatorACL reconstruction surgery with quadriceps tendon autograft
Receives: Procedure: Quadriceps tendon autograft

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Physical examination ACL Failure

    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).

    Measured: 2 years after ACL reconstruction surgery

Secondary outcomes (13)
  1. quality of life (ACL-QoL)

    level of self-reported quality of life

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

  2. functional knee and health status (IKDC)

    level of functional knee and current health status

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

  3. physical examination of knee (in)stability

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

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

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

    self-reported level of physical activity in daily life

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

  5. sports intensity questionnaire (Tegner Activity Level)

    self-reported level of pivoting sports execution

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

  6. questionnaire

    level of physical activity (Lysholm score)

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

  7. knee pain

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

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

  8. Instability knee

    VAS score (patient perception)

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

  9. satisfaction with result of ACL surgery

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

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

  10. physical examination

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

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

  11. physical examination

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

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

  12. Lachman test

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

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

  13. Degree of Osteoarthritis on x-ray

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

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

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Mar 2017
  2. Study start6 Mar 2017
  3. Primary completionDec 2031 (estimated)
  4. Study completionDec 2031 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Randomized controlled trial
Masking
None (open label)
Enrolment
439 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03073083
Sponsor's protocol ID
NL52749.044.16
Acronym
Grafttype
Status last verified
Nov 2025
First submitted
23 Feb 2017
Last updated
25 Nov 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Boer BC, Brouwer RW, Olde Heuvel J, de Vries AJ, van der Wal WA, Christiaan Rompen J, van Houten AH, Hoogeslag RAG. Quadriceps tendon autograft is not inferior to bone-patellar tendon-bone or hamstring autograft in anterior cruciate ligament reconstruction in terms of subjective patient-reported outcomes: Two-year results of a multicenter randomised controlled study. Knee Surg Sports Traumatol Arthrosc. 2026 Feb 27. doi: 10.1002/ksa.70354. Online ahead of print.

    PubMed 41758993

Questions about this trial

What is this clinical trial studying?

A study testing Hamstring tendon autograft, Pattella tendon autograft and Quadriceps tendon autograft in people with Anterior Cruciate Ligament Injuries, run by Orthopedisch Centrum Oost Nederland at 2 sites in Netherlands.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 14 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 25 Nov 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Physical examination ACL Failure (time frame: 2 years after ACL reconstruction surgery). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03073083, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Nov 2025.

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