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.
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
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.
- Conditions
- Anterior Cruciate Ligament Injuries
- 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 group | Role | What they receive |
|---|---|---|
| Hamstring tendon autograft | Active comparator | ACL reconstruction surgery with hamstring tendon autograft Receives: Procedure: Hamstring tendon autograft |
| Patella tendon autograft | Active comparator | ACL reconstruction surgery with pattella tendon autograft Receives: Procedure: Pattella tendon autograft |
| Quadriceps tendon autograft | Active comparator | ACL 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.
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)
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
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
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
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
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
questionnaire
level of physical activity (Lysholm score)
Measured: preoperative, 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery
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
Instability knee
VAS score (patient perception)
Measured: preoperative, 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery
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
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
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
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
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.
- First posted8 Mar 2017
- Study start6 Mar 2017
- Primary completionDec 2031 (estimated)
- Study completionDec 2031 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Anterior Cruciate Ligament InjuriesStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Orthopedisch Centrum Oost Nederland
- Sponsor type
- University, hospital or other
- Collaborators
- Martini Hospital Groningen, Gelderse Vallei Hospital
- Responsible party
- Sponsor
- Investigators
- R.A.G Hoogeslag, MD, Principal investigator, OCON
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
Study at a glance
From the registry record, last updated by the sponsor on 25 Nov 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Graft Selection in Anatomic Anterior Cruciate Ligament Reconstruction: Patella, Hamstrings or Quadriceps Tendon Autograft
- ClinicalTrials.gov ID
- NCT03073083
- Acronym / sponsor ID
- Grafttype / NL52749.044.16
- Conditions
- Anterior Cruciate Ligament Injuries
- Keywords
- autograft
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 439 participants (estimated)
- Lead sponsor
- Orthopedisch Centrum Oost NederlandUniversity, hospital or other
- Collaborators
- Martini Hospital Groningen, Gelderse Vallei Hospital
- Study start
- 6 Mar 2017 (actual)
- Primary completion
- Dec 2031 (estimated)
- Study completion
- Dec 2031 (estimated)
- First posted
- 8 Mar 2017 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
- Model description
- Randomized controlled trial
| Arm | Type | Receives |
|---|---|---|
| Hamstring tendon autograft | Active comparator | Procedure: Hamstring tendon autograftACL reconstruction surgery with hamstring tendon autograft |
| Patella tendon autograft | Active comparator | Procedure: Pattella tendon autograftACL reconstruction surgery with pattella tendon autograft |
| Quadriceps tendon autograft | Active comparator | Procedure: Quadriceps tendon autograftACL reconstruction surgery with quadriceps tendon autograft |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- 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
Key exclusion criteria (14 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Hamstring tendon autograftAlso: all-inside AMPS technique ArthrexACL reconstruction surgery with hamstring tendon | Procedure or surgery | Hamstring tendon autograft |
| Pattella tendon autograftAlso: Smith and NephewACL reconstruction surgery with patella tendon | Procedure or surgery | Patella tendon autograft |
| Quadriceps tendon autograftAlso: all-inside AMPS technique ArthrexACL reconstruction surgery with quadriceps tendon | Procedure or surgery | Quadriceps tendon autograft |
Primary outcome
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).
13 secondary outcomes
quality of life (ACL-QoL)
Time frame: preoperative, 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery
functional knee and health status (IKDC)
Time frame: preoperative, 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery
physical examination of knee (in)stability
Time frame: preoperative, 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery
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
sports intensity questionnaire (Tegner Activity Level)
Time frame: preoperative, 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery
questionnaire
Time frame: preoperative, 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery
knee pain
Time frame: preoperative, 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery
Instability knee
Time frame: preoperative, 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery
satisfaction with result of ACL surgery
Time frame: 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery
physical examination
Time frame: 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery
physical examination
Time frame: preoperative, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery
Lachman test
Time frame: 6 wks, 6 months, 9 months, 1, 2, 5 10 years after ACL reconstruction surgery
Degree of Osteoarthritis on x-ray
Time frame: Baseline, 1,2,5 10 years after ACL reconstruction surgery
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 25 Nov 2025.
- Derived from this study: PubMed 41758993Boer 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.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
R.A.G Hoogeslag, MD principal investigator
OCON
2 sites in 1 country: see every site and its status.
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.