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NCT Number: NCT06357091

ACL Reconstruction With Shark Screw® or Biocomposite-interference Screws

The goal of this clinical trial is to compare the outcome of 2 different screws for Anterior cruciate ligament reconstruction. The main question is if the human allogeneic cortical bone screw reduces tunnel widening in comparison to conventional treatment with a biocomposite screw. Additional the re-rupture rate will be evaluated and knee scores will be recorded before surgery and after surgery. Participants will have MRI before and after surgery, 3, 6, 12, and 24 months after surgery and Computertomography after surgery, 3, 6 and 24 months after surgery. Questionnaires (Knee-scores) will be recorded before surgery, 6, 12, 24 months after surgery.

the investigators hope that with the human cortical bone screw the tunnel widening is reduced and the re-rupture rate is low

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Bezirkskrankenhaus Schwaz Betriebsgesellschaft m.b.H

Schwaz, Tyrol, 6130, Austria

Location status: Recruiting

Location contact

Alexander Rofner-Moretti, MD

CONTACT

[email protected]

+435242600

Alexander Rofner-Moretti, MD

PRINCIPAL_INVESTIGATOR

Boris Tirala, MD

SUB_INVESTIGATOR

Clemens Lottersberger, MD

SUB_INVESTIGATOR

Edith Reches, MD

SUB_INVESTIGATOR

Lukas Pöhl, MD

SUB_INVESTIGATOR

Markus Reichkendler, MD

CONTACT

[email protected]

+435242600

Markus Reichkendler, MD

SUB_INVESTIGATOR

Martin Wallner, MD

SUB_INVESTIGATOR

Samuel Dolling, MD

SUB_INVESTIGATOR

About this study

Rupture of the anterior cruciate ligament of the knee joint is a common (sports) injury in young adults . Depending on various patient-related factors, such an injury can be treated surgically or conservatively . Arthroscopic and anatomical reconstruction is currently considered the gold standard of surgical treatment. In this procedure, the torn anterior cruciate tendon will be replaced usually with the own semitendinosus ligament, the patellar ligament or the quadriceps tendon by inserting it through bone tunnels in the femur and tibia.

However, the optimal technique for fixing the graft remains unclear. Until the replacement graft has healed, the suspension of the graft remains the weak point of the overall construct . The currently common procedures are fixation by means of interference screw in the bone tunnels and distal fixation using endobuttons. These fixation methods differ only insignificantly in clinical scores, stability, or failure rate .

A frequent complication after reconstruction of the anterior cruciate ligament is secondary tunnel dilatation, which has been described in up to 84% of cases. The cause of this is not yet fully understood. Nakazato et al. cites a longer graft and an increased dorsolateral tibial slope. Taketomi makes the posterior tibial slope particularly responsible for tibial tunnel widening and describes that an osteolysis process occurs due to the penetration of synovial fluid into the space between the tendon and the tunnel . Moon et al. see a negative correlation between the length of the graft insertion and tunnel dilation. The widening of the bone tunnels seem not to induce instability, but complicates a follow-up operation, e.g. a new cruciate ligament plasty in the event of rerupture following new trauma. The often up to twice as large bone tunnels make it difficult to find sufficient bone tissue to create a new tunnel. If the already existing and enlarged tunnel is reused, there is a risk of inadequate fixation and lack of incorporation of the new graft. In the revision, a two-stage procedure is often necessary, especially in the case of pronounced widening of the bone tunnel. The group postulates that with a tunnel width >14 mm, only a two-stage procedure is possible. In a first operation, the bone tunnel must be filled with autologous or similar, and only in a second session a new reconstruction of the anterior cruciate ligament can be attempted.

the investigators are planning a prospective, randomized, controlled, single-blind and monocentric study with 2 parallel groups to investigate an alternative fixation method in cruciate ligament surgery. This involves a screw made from allogenic bone (Shark Screw ACL®; Surgebright GmbH, A-4040 Lichtenberg, Austria) in the form of an interference screw obtained from donor cortical bone. The insertion of this bone screw is identical to the usual interference screws. This type of osteosynthesis material has already proven in other forms in fracture treatment. The investigators have been using screws made from allogenic bone in a similar form for the treatment of scaphoid fractures for more than 4 years , Calcaneal fractures, corrective osteotomies, and arthrodesis with excellent success in everyday clinical practice. Treatment with an allogenic bone screw is compared with the current standard treatment with resorbable interference screw MectaScrew (composite), Medacta Int. Str. Regina 34, 6874 Castel San Pietro, Switzerland) in a control group. The aim is to include 80 patients who will be included in the study, i.e. 40 per group. Surgical method, treatment plan and follow up treatment do not differ.

The main objective of the planned study is to analyze the dilation of the bone tunnels in the two groups. This will be done by means of magnetic resonance imaging (MRI) and computer tomography (CT) examinations (MRI preoperatively, postoperatively (within 3 days) and at 6, 12 and 24 months after surgery, CT postoperatively within 3 days and at 6 and 24 months after surgery). The bone tunnels are measured and the results of the two groups are compared to determine whether the allograft screw shows less bone tunnel dilation than the current standard treatment. An initial evaluation of the data and publication is planned after 12 months; the final evaluation and publication will take place after 24 months. The secondary objectives are to record the advantages and disadvantages of the allografts and to analyze their safety and effectiveness. In particular, the incorporation of the screws is to be assessed and classified. In order to better assess the outcome of the operation, clinical parameters will be recorded, and the two groups compared with each other. Furthermore, MRI will be analyzed for its informative value with regard to bone tunnel measurement.

The null hypothesis is that the two surgical procedures (bone screw / biocomposite screw) do not differ in outcome. The alternative hypothesis is that the use of the human, allogenic cortical bone screw as a fixation element for anterior cruciate ligament reconstruction results in faster and, above all, better incorporation of the graft, with less widening of the bone tunnel. Based on the experience of the investigators with similar osteosynthesis material made from allogenic bone, it is to be expected that the bone tunnel will heal scare free. The investigators see the advantage of the proposed treatment particularly in its bone-sparing nature. It is to be expected that this will make possible revision easier and that a two-stage procedure will be necessary less often.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • MRI-verified rupture of the anterior cruciate ligament
  • Indication for replacement surgery
  • Surgery within 6 months of injury
  • Uninjured contralateral knee

Exclusion criteria

  • Previous rupture of the anterior cruciate ligament on the side to be operated on (rerupture)
  • Primary bone disease
  • inflammatory disease
  • Unstable meniscus
  • complete rupture of a collateral ligament
  • early rerupture during the examination period (early rerupture)

Treatment and study plan

ACL reconstruction with Shark Screw ACL®

Procedure

ACL reconstruction with the Shark Screw ACL®, Investigation of tunnel widening

ACL reconstruction with biocomposite screw (Mecta)

Procedure

ACL reconstruction with biocomposite screw (Mecta), Investigation of tunnel widening

Primary outcomes

  1. bone tunnel widening will be measured by CT and/or MRI and measured in mm

    Time frame: immadiately after surgery, 3, 6, 12 and 24 months after surgery.

    bone tunnel widening will be evaluated and measured by CT and/or MRI and measured in mm

Secondary outcomes

  1. International Knee Documentation Committee (IKDC) Scores

    Time frame: before surgery and 6, 12 and 24 months after surgery

    IKDC will be evaluated by questionnaires, it can be between 0 and 100 the higher the better is the outcome

  2. Knee Injury and Osteoarthritis Outcome Score (KOOS) Scores

    Time frame: before surgery and 6, 12 and 24 months after surgery

    KOOS Score will be evaluated by questionnaires, it can be between 0 and 100 the higher the better is the outcome

  3. Lysholm Knee Score

    Time frame: before surgery and 6, 12 and 24 months after surgery

    Lysholm Knee Score will be evaluated by questionnaires, one of the most frequently used assessment tools for the results of Anterior cruciate ligament reconstruction even though it only measures activities of daily living, it can be between 0 and 100 the higher the better is the outcome.

  4. Tegner Activity Score

    Time frame: before surgery and 6, 12 and 24 months after surgery

    Tegner Activity Score will be evaluated by questionnaires

Study contacts

Contact information is provided by the study sponsor or research team.

Alexander Rofner-Moretti, MD

CONTACT

[email protected]

+435242600

Markus Reichkendler, MD

CONTACT

[email protected]

+435242600

Sponsors and collaborators

Lead sponsor

Alexander Rofner-Moretti

Other

Registry information

Official study title

ACL Reconstruction With Human Allograft Cortical Bone Screw (Shark Screw®) or Biocomposite-interference Screws - a Prospective, Randomized, Controlled Trial.

Important dates

Study start
2026
Primary completion
2034
Study completion
2034
First posted
Apr 10, 2024
Registry last updated
Jan 21, 2026

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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