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Anterior Cruciate Ligament InjuryROTORNCT02310854

Acute Anterior Cruciate Ligament Rupture; RecOnsTruction Or Repair?

A study testing ACL Repair and ACL reconstruction in people with Anterior Cruciate Ligament Injury, run by Orthopedisch Centrum Oost Nederland at 1 site in Netherlands.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

To investigate the hypothesis that suture repair of a ruptured vkb, combined with a dynamic intraligamentary stabilization and microfracture of the femoral notch, results in at least equal effectiveness compared with an ACL reconstruction using autologous hamstring in terms of functional recovery one year… Read more about this study

Who is it for?
Ages 18 to 30 years
Conditions the study is for
Anterior Cruciate Ligament Injury
What is being tested?
ACL Repair and ACL reconstruction
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
48 participants
Where
1 siteNetherlands
Study dates
Nov 2014to 17 Apr 2026
Phase
Interventional
Are there results?
None posted in the registry

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 to 30 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Sportive, active patient (Tegner score =/>5)
  • Age above 18 untill 30 years at time of inclusion
  • Primary rupture of the anterior cruciate ligament, evidence by history (acute trauma, clicking sensation, swelling within a few hours, instability) and physical examination (positive Lachman, anterior drawer test and/or Pivot shift)
  • Primary rupture indicated by MRI
  • No associated ligamentuous disorde of the knee, evidenced by history, physical examination, x-ray or MRI)
  • Time span between anterior cruciate ligament rupture and operation no longer than 21 days
  • Willingness to comply to advised rehabilitation protocol supervised by (NFVS registrated) sports physiotherapist

Who cannot join

  • Infection
  • Known hypersensitive response for materials used (Cobalt, chroom, nickel)
  • Serieus pre-existing malaligment of leg indicated for surgery
  • Tendency for excessive scar tisseu formation, such as arthrofibrosis
  • History of previous surgery on leg indicated for surgery
  • History of removal of tendon on leg indicated for surgery
Show all 12Show fewer
  • Muscular, neurological or vascular disorders negatively affecting healing or rehabilitation
  • Cartilage injury requiring (some kind of) cartilage repair surgery (such as microfracture or cell therapy)
  • Arthrosis more dan ICRS grade 2 evidenced by x-ray
  • Long(er) term use of relevant medication, such as prednisolon or cytostatica
  • Pregnancy
  • Know osteoporosis

Trial locations and contacts

1 site in 1 country.

Netherlands1 site
  • Orthopedisch Centrum Oost Nederland /ZGT

    Hengelo, 7555

Other trials in Netherlands

About this study

To investigate the hypothesis that suture repair of a ruptured vkb, combined with a dynamic intraligamentary stabilization and microfracture of the femoral notch, results in at least equal effectiveness compared with an ACL reconstruction using autologous hamstring in terms of functional recovery one year postoperatively in terms of a patient self-reported outcome related to be able to conduct daily and sporting activities. Secondary, the evaluation of clinical outcomes, self-reported by the patient outcomes, osteoarthritis, rehabilitation time required for return to daily and sporting activities and levels of sporting activity which has returned in patients with status after an ACL rupture and suture repair augmented with a dynamic intraligamentary microfracture and stabilization of the femoral notch in comparison with an anterior cruciate ligament reconstruction with the ipsilateral hamstring graft.

Read the detailed description

Background of the study:

An anterior cruciate ligament rupture is a serious injury to the knee with high probability of the occurrence of dynamic instability, accompanying lesions and early post-traumatic arthrosis. Despite conservative treatment through rehabilitation or ACL reconstruction surgery not all patients do return to their previous activity levels. Moreover degenerative changes, especially early posttraumatic arthrosis, are not counteracted.

In order to optimize the clinical results after ACL surgery, a renewed interest has emerged in healing the patient's own ruptured ACL after attaching. Literature suggests that with the current innovations in surgical repair techniques of (natural) healing of a ruptured ACL may result in similar clinical outcomes in comparison to the gold standard, the ACL reconstruction. In addition, it may even reduce degenerative changes occur in relation to the gold standard. Moreover, the return to daily activities and sports level seems significantly faster than after ACL reconstruction.

The hypothesis is that a suture (suture repair) of a ruptured ACL, combined with a dynamic intraligamentary stabilization, as well as microfracture of the femoral notch, passes, at least equal efficacy in comparison with an anterior cruciate ligament reconstruction using autologous hamstrings in terms of functional recovery 1 years postoperatively.

The DIS bonding technique will be applied in the current study to surgically repair (suture) the ruptured ACL. DIS is an abbreviation and stands for intraligamentary dynamic stabilization (DIS). DIS has been used in humans and seems to provide a high patient satisfaction, favorable clinical and radiological results. However, to our knowledge, to date, no randomized comparative study has been conducted yet in which the DIS technique is compared with the gold standard, the ACL reconstruction.

Objective of the study:

Primary goal:

Investigate the hypothesis that suture repair of a ruptured vkb, combined with a dynamic intraligamentary stabilization and microfracture of the femoral notch, results in at least equal effectiveness compared with an ACL reconstruction using autologous hamstring in terms of functional recovery one year postoperatively in terms of a patient self-reported outcome related to be able to conduct daily and sporting activities.

Secondary objective:

Evaluation of clinical outcomes, self-reported by the patient outcomes, osteoarthritis, rehabilitation time required for return to daily and sporting activities and levels of sporting activity which has returned in patients with status after an ACL rupture and suture repair augmented with a dynamic intraligamentary microfracture and stabilization of the femoral notch in comparison with an anterior cruciate ligament reconstruction with the ipsilateral hamstring graft.

Study design:

This study is a single center stratified block randomized controlled trial. Patients with ACL rupture, confirmed by an orthopedic surgeon based on the outpatient history and radiographic images, will be randomized into an experimental ('repair' / DIS) group after inclusion and a control (reconstruction, regular care) group. Patients will be stratified on the level of sport/physical active practice, on the basis of the Tegner score. The Tegner score is an evaluative and inventory questionnaire on which the patient indicates the gravity of his work and/or sports activities. A higher score is associated with a higher level of physical strain/activity . On the basis of the Tegner score patients will be stratified into a 'moderate' physically active stratum (group Tegner score 5-6-7) and 'highly' physically active stratum (group Tegner score 8 -9-10). Stratification based on the degree of physical activity is considered to be important because the extent and severity of physical activity/strain in daily life poses a potential (difference) in risk of re-rupture between the two study arms. In order to minimize potential differences in 'exposure' or 'risk of re-rupture' between the two study groups stratification is relevant.Measurements take place at baseline, peri-operative / immediately after surgery, 6 weeks, 3,6,9 months and 1, 2, 5 and 10 years postoperatively.

Study population: (Physically) active patients from 18 untill 30 years, who has visited the outpatient clinic of the orthopedic surgeon because of a knee injury resulting in a ACL rupture, for whom surgery indication for an ACL reconstruction exists and who can be operated on within three weeks after the onset of the ACL rupture.

Intervention:

n=48 patients will participate in the current study. Patients will be assigned to a suture repair of the ruptured vkb complemented by a dynamic intraligamentary stabilization (DIS) and microfracture of the femoral notch or the gold standard, a ACL reconstruction.

Primary study parameters/outcome of the study:

Self-reported functional outcome at one-year follow post surgery measured by the IKDC 2000 subjective scale.

Secundary study parameters/outcome of the study (if applicable):

Secondaire eindpunten: Self-reported functional outcome at one-year follow post surgery measured by the IKDC 2000 subjective scale 6 weeks, 3,6 and 9 months, 2,5 and 10 years post surgery, self-reported disabilities (KOOS), level of physical activity (Tegner), satisfaction (VAS) as well as IKDC physical examination (clinimetretrics) 6 weeks, 3, 6 en 9 months, 1, 2, 5 and 10 years post surgery; instrumented anteroposterior laxity, leg symmetry index for jump tests as well as isokinetic quadriceps en hamstrings force 6 en 9 months, 1, 2, 5 en 10 years after surgery; radiologic signs of arthrosis 1,2 5 and 10 years post surgery; reruptures of the ACL within 10 years post surgery, classification rupture pattern peroperative.

Being tested
ACL Repair, ACL reconstruction
Keywords
anterior cruciate ligament rupture, autograft, reconstruction, orthopedic surgery, dynamic intraligament stabilization
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.

  • ACL RepairProcedure or surgery

    Also called Dynamic Intraligament Stabilization (DIS), Augmented suture

    augmented suture of acute ACL rupture (<3 weeks after injury)

  • ACL reconstructionProcedure or surgery

    Also called Primary ACL reconstruction, Autograft hamstring, All-inside

    reconstruction hamstring autograft

Study groups in NCT02310854
Study groupRoleWhat they receive
ACL ReconstructionActive comparatorPrimary reconstructive surgery of ACL with hamstring autograft (All-inside, Arthrex, Napels, Florida, USA)
Receives: Procedure: ACL reconstruction
ACL RepairExperimentalPrimary augmented suture of ACL using Dynamic Intraligament Stabilization (DIS; Mathys Medical Bettlach, Switzerland)
Receives: Procedure: ACL Repair

What is being measured

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

  1. IKDC 2000 subjective knee evaluation form

    questionniare/self-reported functional limitations in activitities of daily living and/or sports activities

    Measured: baseline, 12 months post surgery

Secondary outcomes (6)
  1. IKDC 2000 subjective knee evaluation form

    questionnaire/self-reported functional limitations in activitities of daily living and/or sports

    Measured: baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery

  2. IKDC 2000 objective knee evaluation form

    knee physical examination form / clinimetrics

    Measured: baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery

  3. Knee Injury and Osteoarthritis Outcome Score (KOOS)

    questionnaire designed to assess short and long term patient-related ouctome following knee injury on pain, symptoms, activities of daily living, sport and recreation, knee-related quality of life

    Measured: baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery

  4. Tegner Activity Level Scale

    Rating scale to determine the type and intensity of sports/activities

    Measured: baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery

  5. Instrumented anteroposterior laxity

    Measured: baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery

  6. LSI jump-force testing

    leg symmetry index for jump tests as well as isokinetic quadriceps and hamstring force tests

    Measured: 6-9-12 months, 2-5-10 years post 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 Dec 2014 (estimated)
  2. Study startNov 2014
  3. Primary completionApr 2026
  4. Study completion17 Apr 2026

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
Other
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
48 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02310854
Sponsor's protocol ID
NL5011604414
Acronym
ROTOR
Status last verified
Apr 2026
First submitted
1 Dec 2014
Last updated
22 Apr 2026
Results posted
No
Data monitoring committee
Yes
Individual data sharing
Undecided: to be determined yet

Publications

  • Hoogeslag RAG, Brouwer RW, Boer BC, de Vries AJ, Huis In 't Veld R. Acute Anterior Cruciate Ligament Rupture: Repair or Reconstruction? Two-Year Results of a Randomized Controlled Clinical Trial. Am J Sports Med. 2019 Mar;47(3):567-577. doi: 10.1177/0363546519825878.

    PubMed 30822124
  • Boer BC, Hoogeslag RAG, Brouwer RW, Demmer A, Huis In 't Veld RMHA. Self-reported functional recovery after reconstruction versus repair in acute anterior cruciate ligament rupture (ROTOR): a randomized controlled clinical trial. BMC Musculoskelet Disord. 2018 Apr 20;19(1):127. doi: 10.1186/s12891-018-2028-4.

    PubMed 29678170

Questions about this trial

What is this clinical trial studying?

A study testing ACL Repair and ACL reconstruction in people with Anterior Cruciate Ligament Injury, run by Orthopedisch Centrum Oost Nederland at 1 site 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 7 inclusion and 12 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: finished, as of the sponsor's last update on 22 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

IKDC 2000 subjective knee evaluation form (time frame: baseline, 12 months post 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 NCT02310854, which also lists 2 linked publications.

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 22 Apr 2026.

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