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NCT Number: NCT02918734

Fixation of Patellar Tendon Grafts in Anterior Cruciate Ligament Reconstruction. Endobutton vs Metal Interference Screws

In this randomized controlled trial the investigators will compare the results after primary anterior cruciate ligament (ACL) reconstruction using two different methods for femoral fixation of a bone-patellar tendon-bone (BPTB) autograft. Interference screws have been the standard method for fixing the femoral side of BPTB grafts; however, several pitfalls have been reported. Cortical fixation with the Endobutton CL BTB Fixation System has become available and the clinical results have been described as promising; however, no randomized controlled trials comparing these two femoral fixation methods have been conducted, and there is no published data that confirms that the bone block heals in the tunnel with the newer method.

The aim of our study is to compare the outcome after primary ACL reconstruction with BPTB autografts using the Endobutton CL BTB or metal interference screw for femoral fixation.

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Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Orthopedic Surgery, St Olavs Hospital, Trondheim, Norway

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About this study

Primary anterior cruciate ligament (ACL) reconstructions with bone-patellar tendon-bone (BPTB) autografts have recently been found to have a lower risk of revision compared with hamstring tendon autografts, and BPTB has again become our graft of choice. Interference screws have been the standard method for fixing the femoral side of a BPTB graft; however problems such as damage of the graft and failure due to nonparallel screw placement have been reported. Cortical fixation using a suspensory system has been used for soft-tissue graft fixation for several years, and a corresponding device, the Endobutton CL BTB Fixation System (Smith & Nephew, Inc., Andover, MA, USA), has become available for fixation of bone-tendon-bone grafts. The clinical results after fixation with the Endobutton CL BTB have been described as promising; however, no randomized controlled trials comparing these two fixation methods have been conducted, and there is no published data that confirms that the bone block heals in the tunnel with the newer method.

In this randomized controlled trial, patients undergoing primary ACL reconstruction will be randomized into either an Endobutton group or an interference screw group. The primary aim of the study is to compare these two fixation methods, assessed by patient reported outcomes, laxity, range of motion and muscle strength. Knee related quality of life 2 years after surgery is the primary outcome, measured by the Knee injury and Osteoarthritis Outcome Score (KOOS) subscale "knee related Quality of life (QOL)". Other aims are to see if there is any difference in the integration of the bone block in the femoral tunnel assessed by CT scan, in the risk of developing osteoarthritis assessed by radiographs, or in the risk of a postoperative complication or revision. The patients will be followed up 6 weeks, 6 months, 2 years and 10 years after surgery. CT scan will be performed after 6 months, and radiographs after 2 years and 10 years. In addition details of the rehabilitation will be recorded. Patients undergoing a revision will be followed up but excluded from further comparisons in the study.

Our hypothesis is that there is no difference in the outcome after primary ACL reconstruction with BPTB autografts using the Endobutton CL BTB or metal interference screw for femoral fixation, both with a metal interference screw for the tibial fixation.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Primary reconstruction of ACL ruptures
  • Surgery at least 6 weeks after injury
  • The patient must accept and sign the informed consent form before surgery

Exclusion criteria

  • Medical indication for using another graft than BPTB autograft (such as history of anterior knee pain or occupations etc. requiring frequent kneeling)
  • Previous major surgical procedures in the same knee
  • Major additional injuries in the knee (posterior cruciate ligament, lateral collateral ligament, medial collateral ligament, sutured meniscus lesions and major cartilage lesions undergoing cartilage repair)
  • Contralateral ACL injury (treated or untreated)
  • Present or former serious illness that makes follow-up or rehabilitation difficult (e.g. alcohol or drug abuse, psychiatric disease)

Treatment and study plan

Endobutton CL BTB

Device

ACL reconstruction with Endobutton CL BTB

Metal interference screw

Device

ACL reconstruction with metal interference screw

Primary outcomes

  1. Knee related quality of life

    Time frame: 2 years

    KOOS subscale "knee related Quality of life (QOL)"

Secondary outcomes

  1. Tegner activity scale

    Time frame: 6 months, 2 years, 10 years

  2. Lachman test

    Time frame: 6 weeks, 6 months, 2 years, 10 years

    Anterior translation of the tibia

  3. Muscular strength

    Time frame: 6 months, 2 years, 10 years

    Biodex dynamometer

  4. Bone block integration

    Time frame: 6 months

    CT scan

  5. Osteoarthritis

    Time frame: 2 years, 10 years

    X-ray radiographs

  6. Range of motion

    Time frame: 6 weeks, 6 months, 2 years, 10 years

  7. Knee related quality of life

    Time frame: 6 weeks

    KOOS subscale "knee related Quality of life (QOL)"

  8. Knee related quality of life

    Time frame: 6 months

    KOOS subscale "knee related Quality of life (QOL)"

  9. Knee related quality of life

    Time frame: 10 years

    KOOS subscale "knee related Quality of life (QOL)"

  10. Lysholm functional knee score

    Time frame: 6 weeks, 6 months, 2 years, 10 years

  11. KOOS

    Time frame: 6 weeks, 6 months, 2 years, 10 years

    Knee injury and Osteoarthritis Outcome Score

  12. Pivot shift test

    Time frame: 6 weeks, 6 months, 2 years, 10 years

    Anteroposterior and rotational stability

  13. KT-1000 arthrometer

    Time frame: 6 weeks, 6 months, 2 years, 10 years

    Anterior translation of the tibia

Other outcomes

  1. Complications

    Time frame: Up to 10 years

    Registration

  2. Reoperations

    Time frame: Up to 10 years

    Registration

Study contacts

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

Tone Gifstad, md phd

CONTACT

[email protected]

Trond Olav Lundemo, md

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

St. Olavs Hospital

Other

Collaborators

  • Rosenborgklinikken

Registry information

Official study title

A Prospective Randomized Controlled Trial Comparing the Endobutton CL BTB Fixation System With Metal Interference Screws in the Femoral Fixation of Patellar Tendon Grafts in Anterior Cruciate Ligament Reconstruction.

Important dates

Study start
2016
Primary completion
2026
Study completion
2033
First posted
Sep 29, 2016
Registry last updated
Jul 20, 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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