Fixation of Patellar Tendon Grafts in Anterior Cruciate Ligament Reconstruction. Endobutton vs Metal Interference Screws
Primary Purpose
Knee Injuries
Status
Recruiting
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Endobutton CL BTB
Metal interference screw
Sponsored by
About this trial
This is an interventional treatment trial for Knee Injuries focused on measuring Anterior Cruciate Ligament, Bone-Patellar Tendon-Bone Grafting
Eligibility Criteria
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)
Sites / Locations
- Department of Orthopedic Surgery, St Olavs HospitalRecruiting
- RosenborgklinikkenRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Endobutton CL BTB
Metal interference screw
Arm Description
Femoral fixation of the BPTB autograft with the Endobutton CL BTB Fixation System.
Femoral fixation of the BPTB autograft with a metal interference screw.
Outcomes
Primary Outcome Measures
Knee related quality of life
KOOS subscale "knee related Quality of life (QOL)"
Secondary Outcome Measures
Tegner activity scale
Lachman test
Anterior translation of the tibia
Muscular strength
Biodex dynamometer
Bone block integration
CT scan
Osteoarthritis
X-ray radiographs
Range of motion
Knee related quality of life
KOOS subscale "knee related Quality of life (QOL)"
Knee related quality of life
KOOS subscale "knee related Quality of life (QOL)"
Knee related quality of life
KOOS subscale "knee related Quality of life (QOL)"
Lysholm functional knee score
KOOS
Knee injury and Osteoarthritis Outcome Score
Pivot shift test
Anteroposterior and rotational stability
KT-1000 arthrometer
Anterior translation of the tibia
Full Information
NCT ID
NCT02918734
First Posted
June 20, 2016
Last Updated
March 8, 2023
Sponsor
St. Olavs Hospital
Collaborators
Rosenborgklinikken
1. Study Identification
Unique Protocol Identification Number
NCT02918734
Brief Title
Fixation of Patellar Tendon Grafts in Anterior Cruciate Ligament Reconstruction. Endobutton vs Metal Interference Screws
Official 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.
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 2016 (Actual)
Primary Completion Date
March 2025 (Anticipated)
Study Completion Date
March 2033 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
St. Olavs Hospital
Collaborators
Rosenborgklinikken
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
Detailed Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Injuries
Keywords
Anterior Cruciate Ligament, Bone-Patellar Tendon-Bone Grafting
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
220 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Endobutton CL BTB
Arm Type
Experimental
Arm Description
Femoral fixation of the BPTB autograft with the Endobutton CL BTB Fixation System.
Arm Title
Metal interference screw
Arm Type
Active Comparator
Arm Description
Femoral fixation of the BPTB autograft with a metal interference screw.
Intervention Type
Device
Intervention Name(s)
Endobutton CL BTB
Intervention Description
ACL reconstruction with Endobutton CL BTB
Intervention Type
Device
Intervention Name(s)
Metal interference screw
Intervention Description
ACL reconstruction with metal interference screw
Primary Outcome Measure Information:
Title
Knee related quality of life
Description
KOOS subscale "knee related Quality of life (QOL)"
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Tegner activity scale
Time Frame
6 months, 2 years, 10 years
Title
Lachman test
Description
Anterior translation of the tibia
Time Frame
6 weeks, 6 months, 2 years, 10 years
Title
Muscular strength
Description
Biodex dynamometer
Time Frame
6 months, 2 years, 10 years
Title
Bone block integration
Description
CT scan
Time Frame
6 months
Title
Osteoarthritis
Description
X-ray radiographs
Time Frame
2 years, 10 years
Title
Range of motion
Time Frame
6 weeks, 6 months, 2 years, 10 years
Title
Knee related quality of life
Description
KOOS subscale "knee related Quality of life (QOL)"
Time Frame
6 weeks
Title
Knee related quality of life
Description
KOOS subscale "knee related Quality of life (QOL)"
Time Frame
6 months
Title
Knee related quality of life
Description
KOOS subscale "knee related Quality of life (QOL)"
Time Frame
10 years
Title
Lysholm functional knee score
Time Frame
6 weeks, 6 months, 2 years, 10 years
Title
KOOS
Description
Knee injury and Osteoarthritis Outcome Score
Time Frame
6 weeks, 6 months, 2 years, 10 years
Title
Pivot shift test
Description
Anteroposterior and rotational stability
Time Frame
6 weeks, 6 months, 2 years, 10 years
Title
KT-1000 arthrometer
Description
Anterior translation of the tibia
Time Frame
6 weeks, 6 months, 2 years, 10 years
Other Pre-specified Outcome Measures:
Title
Complications
Description
Registration
Time Frame
Up to 10 years
Title
Reoperations
Description
Registration
Time Frame
Up to 10 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Trond Olav Lundemo, md
Email
trond.olav.lundemo@stolav.no
First Name & Middle Initial & Last Name or Official Title & Degree
Tone Gifstad, md phd
Email
tone.gifstad@stolav.no
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jon Olav Drogset, md phd
Organizational Affiliation
St. Olavs Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Orthopedic Surgery, St Olavs Hospital
City
Trondheim
Country
Norway
Individual Site Status
Recruiting
Facility Name
Rosenborgklinikken
City
Trondheim
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Agnar Tegnander, md phd
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Fixation of Patellar Tendon Grafts in Anterior Cruciate Ligament Reconstruction. Endobutton vs Metal Interference Screws
We'll reach out to this number within 24 hrs