An interventional study of Endobutton CL BTB and Metal interference screw in Knee Injuries, sponsored by St. Olavs Hospital. Recruiting at 2 sites in Norway. Open to participants aged 18 Years to 55 Years. Per ClinicalTrials.gov, last updated 2026-07-20.
Sponsored by St. Olavs Hospital · Not applicable, Interventional, and Treatment
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.
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.
249 studies on the registry are indexed under Knee Injuries; 48 are open to participants now.
This study's planned enrollment of 220 is above the median of 50 across 160 interventional studies indexed under Knee Injuries.
Browse Knee Injuries studies →St. Olavs Hospital is the lead sponsor of 165 studies on the registry; 30 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Femoral fixation of the BPTB autograft with the Endobutton CL BTB Fixation System.
Device: Endobutton CL BTB
Femoral fixation of the BPTB autograft with a metal interference screw.
Device: Metal interference screw
ACL reconstruction with Endobutton CL BTB
ACL reconstruction with metal interference screw
Knee related quality of life
KOOS subscale "knee related Quality of life (QOL)"
Time frame: 2 years
Tegner activity scale
Time frame: 6 months, 2 years, 10 years
Lachman test
Anterior translation of the tibia
Time frame: 6 weeks, 6 months, 2 years, 10 years
Muscular strength
Biodex dynamometer
Time frame: 6 months, 2 years, 10 years
Bone block integration
CT scan
Time frame: 6 months
Osteoarthritis
X-ray radiographs
Time frame: 2 years, 10 years
Range of motion
Time frame: 6 weeks, 6 months, 2 years, 10 years
Knee related quality of life
KOOS subscale "knee related Quality of life (QOL)"
Time frame: 6 weeks
Knee related quality of life
KOOS subscale "knee related Quality of life (QOL)"
Time frame: 6 months
Knee related quality of life
KOOS subscale "knee related Quality of life (QOL)"
Time frame: 10 years
Lysholm functional knee score
Time frame: 6 weeks, 6 months, 2 years, 10 years
KOOS
Knee injury and Osteoarthritis Outcome Score
Time frame: 6 weeks, 6 months, 2 years, 10 years
Pivot shift test
Anteroposterior and rotational stability
Time frame: 6 weeks, 6 months, 2 years, 10 years
KT-1000 arthrometer
Anterior translation of the tibia
Time frame: 6 weeks, 6 months, 2 years, 10 years
Complications
Registration
Time frame: Up to 10 years
Reoperations
Registration
Time frame: Up to 10 years
Plan to share: No
No publications or documents are linked to this record.
Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.
Contact study teamGet an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
St. Olavs Hospital