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Comparison of Three Methods for Anterior Cruciate Ligament Reconstruction

Primary Purpose

Anterior Cruciate Ligament Rupture, Deficiency of Anterior Cruciate Ligament, Chronic Instability of Knee

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Patellar Tendon
Hamstring Tendon
Double-Bundle
Sponsored by
University of Calgary
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anterior Cruciate Ligament Rupture focused on measuring Anterior Cruciate Ligament (ACL) Reconstruction, Patellar Tendon, Hamstring Tendon, Double-Bundle, Autograft

Eligibility Criteria

14 Years - 50 Years (Child, Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

A confirmed diagnosis of anterior cruciate ligament deficiency based on all of the following:

  • History of a traumatic injury episode
  • Physical examination findings of increased anterior translation of the tibia on the femur (Lachman test and/or anterior drawer test)
  • A positive pivot shift test
  • X-rays showing skeletal maturity (ie: tibial tubercle fused) and no fractures. (NB: Magnetic resonance imaging is not required)
  • Age 14-50 years old

Exclusion Criteria:

  • Patients with combined ligament deficiencies (Posterior Cruciate, Medial and/or Lateral Collateral deficiency.) (NB: Grade 1 side to side differences (ie. < 5mm) on valgus, varus or posterior stress testing will not be considered exclusions)
  • Intra-operative identification of International Cartilage Repair Society (ICRS) Grade 4 chondral lesion of > 1 cm ² [61]
  • Previous ligament surgery on the affected or contralateral knees
  • Cases involving litigation or Worker's Compensation
  • Confirmed connective tissue disorder (ie: Ehlers-Danlos, Marfans)
  • X-ray showing that tibial physis is not fused

Sites / Locations

  • University of Calgary Sport Medicine Centre

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Patellar Tendon (PT)

Hamstring (HT)

Double-Bundle (DB)

Arm Description

ACL reconstruction using a patellar tendon autograft

ACL reconstruction using a quadruple-strand semitendinosus/gracilis (hamstring) tendon single-bundle autograft

ACL reconstruction using a semitendinosus/gracilis (hamstring) tendon double-bundle autograft

Outcomes

Primary Outcome Measures

Anterior Cruciate Ligament Quality of Life (ACL-QOL) Outcome
The 32-item patient-reported Anterior Cruciate Ligament Quality-of-Life (ACL-QOL) questionnaire assesses symptoms/physical complaints, work-related, sports/recreational, lifestyle and social/emotional concerns. A higher score on the 0 to 100mm visual analog scale represents better quality of life.

Secondary Outcome Measures

Number of Participants With Traumatic ACL Re-ruptures and Atraumatic Graft Failures
COMPLETE TRAUMATIC RE-RUPTURE - defined as a consequence of an acute traumatic event resulting in a change in static stability since the most recent follow-up visit; determined clinically by a definite loss of end point on Lachman testing, increased anterior translation (>3mm) and a greater than or equal grade 2 pivot shift. Confirmed by MRI or diagnostic arthroscopy. PARTIAL TRAUMATIC TEARS - defined as a consequence of an acute traumatic event resulting in a suspected meniscal injury or graft tear on history, without the clinical characteristics of a "complete traumatic rerupture". Confirmed by MR or diagnostic arthroscopy. TRAUMATIC RE-INJURY - combined total of "complete traumatic re-ruptures" and "partial traumatic tears". ATRAUMATIC GRAFT FAILURES - defined in the absence of an acute traumatic event, with greater than or equal grade 2 pivot shift and/or greater than or equal to 6mm side-to-side difference on the KT arthrometer.
Number of Participants With Each International Knee Documentation Committee (IKDC) Objective Overall Group Grade
IKDC Objective group grades: Normal (A), Nearly Normal (B), Abnormal (C), Severely Abnormal (D) The IKDC Objective Overall Group Grade is determined by the lowest grade assigned to defined objective knee examination measurements, including effusion, passive motion deficit and manual/instrumented ligament examinations (i.e. Lachman, anterior-posterior (AP) translation).
Mean International Knee Documentation Committee (IKDC) Subjective Score
Patient-reported health-related outcome measure with a score between 0 and 100. A higher score represents a better outcome.
Number of Participants With Each Pivot Shift Grade
The Pivot Shift test is a dynamic, passive test to assess the rotational instability of the Anterior Cruciate Ligament in the knee. Pivot shift grades include: equal/0 (negative); glide/1; clunk/2; gross/3. A positive grade indicates injury to the Anterior Cruciate Ligament.
Proportion of Patients With Moderate or Severe Kneeling Pain
Patients kneeled down on the same hard surface (i.e. clinic floor) and self-reported the pain on a scale of: none, mild, moderate or severe. The number of patients reporting moderate or severe kneeling pain were combined in the reported proportions.
Knee Laxity as Measured by the KT Arthrometer
Mean side-to-side differences, as measured using the KT-1000 Arthrometer instrument at 30lbs/134N forces to objectively measure knee laxity.
Mean Tegner Activity Level
Tegner Activity Scale (Values indicate level of activity from inactive (Level 0) to competitive level of activity (Level 10))
Return to Pre-injury Tegner Activity Level
Proportion of patients returning to pre-injury levels, as measured by the Tegner Activity Scale (Values indicate level of activity from inactive (Level 0) to competitive level of activity (Level 10)).
Cincinnati Occupational Rating Scale
The Cincinnati Occupational Rating Scale assesses the level of work-related activities, including sitting, standing, walking, squatting, climbing, lifting and carrying weighted objects. The score ranges from 0 to 100, with a lower score representing more sedentary work-related activities.
Skin-to-Skin Operative Times
Skin-to-skin operative times (in minutes) for each ACL reconstruction procedure
Radiographic (X-ray) Changes
The analysis for the radiographic assessment data is currently ongoing, to provide a comparison of baseline, 2- and 5-year post-operative x-rays.

Full Information

First Posted
September 12, 2007
Last Updated
April 27, 2021
Sponsor
University of Calgary
Collaborators
Workers' Compensation Board, Alberta
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1. Study Identification

Unique Protocol Identification Number
NCT00529958
Brief Title
Comparison of Three Methods for Anterior Cruciate Ligament Reconstruction
Official Title
A Randomized Clinical Trial Comparing Three Methods for Anterior Cruciate Ligament Reconstruction: Patellar Tendon, Quadruple Semitendinosus/Gracilis and Double-Bundle Semitendinosus/Gracilis Grafts.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Unknown status
Study Start Date
September 2007 (Actual)
Primary Completion Date
December 2010 (Actual)
Study Completion Date
December 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Calgary
Collaborators
Workers' Compensation Board, Alberta

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this randomized clinical trial is to determine the difference in quality of life outcome at two years, in patients undergoing an Anterior Cruciate Ligament (ACL) reconstruction procedure with either a patellar tendon, quadruple hamstring tendon or a double-bundle hamstring tendon autograft.
Detailed Description
Following an ACL injury, the knee is predisposed to chronic instability, further damage to the meniscal and chondral structures in the knee, osteoarthritis and an impaired quality of life. The successful treatment of an ACL deficient knee aims to preserve the intact meniscus and chondral structures, and to provide a functionally stable knee so that patients can return to pre-injury activities and restore their quality of life. The current standard of care for ACL deficient knees is with a surgical ACL reconstruction procedure. A Cochrane Review was done and demonstrated that the existing literature is controversial. To date, no existing trial has used validated patient-based outcome assessment, accounted for the critical differences between acute and chronic ACL deficiency or used modern techniques to ensure randomization concealment and a sufficient sample size to avoid type II error. The existing information does not define graft failure or re-ruptures, involve long-term follow-up to address osteoarthritis development, nor compare outcomes between single- and double-bundle reconstructive techniques. The current standard includes either a patellar tendon or quadruple semitendinosus/gracilis tendon autograft reconstruction. The newest option is a double-bundle semitendinosus/gracilis graft. This option attempts to restore the complex ACL anatomy by using two separate tendon components to reconstruct the ACL. This study will measure disease-specific quality of life at short- and long-term post-operative intervals (1, 2, 5 and 10 years). Additional secondary outcomes, including the incidence of traumatic re-ruptures and graft failures, will also be compared between treatment groups.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anterior Cruciate Ligament Rupture, Deficiency of Anterior Cruciate Ligament, Chronic Instability of Knee, Anterior Cruciate Ligament Injury
Keywords
Anterior Cruciate Ligament (ACL) Reconstruction, Patellar Tendon, Hamstring Tendon, Double-Bundle, Autograft

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
330 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Patellar Tendon (PT)
Arm Type
Active Comparator
Arm Description
ACL reconstruction using a patellar tendon autograft
Arm Title
Hamstring (HT)
Arm Type
Active Comparator
Arm Description
ACL reconstruction using a quadruple-strand semitendinosus/gracilis (hamstring) tendon single-bundle autograft
Arm Title
Double-Bundle (DB)
Arm Type
Active Comparator
Arm Description
ACL reconstruction using a semitendinosus/gracilis (hamstring) tendon double-bundle autograft
Intervention Type
Procedure
Intervention Name(s)
Patellar Tendon
Other Intervention Name(s)
Bone-patellar tendon-bone graft, BTPB graft
Intervention Description
Patellar Tendon autograft
Intervention Type
Procedure
Intervention Name(s)
Hamstring Tendon
Other Intervention Name(s)
Single-bundle hamstring graft, ST/G graft
Intervention Description
Quadruple Semitendinosus/Gracilis (Hamstring) Tendon Autograft
Intervention Type
Procedure
Intervention Name(s)
Double-Bundle
Other Intervention Name(s)
Double-bundle ST/G graft
Intervention Description
Double-Bundle Semitendinosus/Gracilis (Hamstring) Tendon Autograft
Primary Outcome Measure Information:
Title
Anterior Cruciate Ligament Quality of Life (ACL-QOL) Outcome
Description
The 32-item patient-reported Anterior Cruciate Ligament Quality-of-Life (ACL-QOL) questionnaire assesses symptoms/physical complaints, work-related, sports/recreational, lifestyle and social/emotional concerns. A higher score on the 0 to 100mm visual analog scale represents better quality of life.
Time Frame
Baseline, 3 and 6 months, 1, 2 and 5 years post-operatively
Secondary Outcome Measure Information:
Title
Number of Participants With Traumatic ACL Re-ruptures and Atraumatic Graft Failures
Description
COMPLETE TRAUMATIC RE-RUPTURE - defined as a consequence of an acute traumatic event resulting in a change in static stability since the most recent follow-up visit; determined clinically by a definite loss of end point on Lachman testing, increased anterior translation (>3mm) and a greater than or equal grade 2 pivot shift. Confirmed by MRI or diagnostic arthroscopy. PARTIAL TRAUMATIC TEARS - defined as a consequence of an acute traumatic event resulting in a suspected meniscal injury or graft tear on history, without the clinical characteristics of a "complete traumatic rerupture". Confirmed by MR or diagnostic arthroscopy. TRAUMATIC RE-INJURY - combined total of "complete traumatic re-ruptures" and "partial traumatic tears". ATRAUMATIC GRAFT FAILURES - defined in the absence of an acute traumatic event, with greater than or equal grade 2 pivot shift and/or greater than or equal to 6mm side-to-side difference on the KT arthrometer.
Time Frame
Minimum 2-year Follow-up, and 5-Year Follow-up
Title
Number of Participants With Each International Knee Documentation Committee (IKDC) Objective Overall Group Grade
Description
IKDC Objective group grades: Normal (A), Nearly Normal (B), Abnormal (C), Severely Abnormal (D) The IKDC Objective Overall Group Grade is determined by the lowest grade assigned to defined objective knee examination measurements, including effusion, passive motion deficit and manual/instrumented ligament examinations (i.e. Lachman, anterior-posterior (AP) translation).
Time Frame
Baseline, 1, 2 and 5 years post-operatively
Title
Mean International Knee Documentation Committee (IKDC) Subjective Score
Description
Patient-reported health-related outcome measure with a score between 0 and 100. A higher score represents a better outcome.
Time Frame
Baseline, 3 and 6 months, 1, 2 and 5 years post-operatively
Title
Number of Participants With Each Pivot Shift Grade
Description
The Pivot Shift test is a dynamic, passive test to assess the rotational instability of the Anterior Cruciate Ligament in the knee. Pivot shift grades include: equal/0 (negative); glide/1; clunk/2; gross/3. A positive grade indicates injury to the Anterior Cruciate Ligament.
Time Frame
Baseline, 3 and 6 months, 1, 2 and 5 years post-operatively
Title
Proportion of Patients With Moderate or Severe Kneeling Pain
Description
Patients kneeled down on the same hard surface (i.e. clinic floor) and self-reported the pain on a scale of: none, mild, moderate or severe. The number of patients reporting moderate or severe kneeling pain were combined in the reported proportions.
Time Frame
Baseline, 2 and 5 years post-operatively
Title
Knee Laxity as Measured by the KT Arthrometer
Description
Mean side-to-side differences, as measured using the KT-1000 Arthrometer instrument at 30lbs/134N forces to objectively measure knee laxity.
Time Frame
Baseline, 1 and 2 years post-operatively
Title
Mean Tegner Activity Level
Description
Tegner Activity Scale (Values indicate level of activity from inactive (Level 0) to competitive level of activity (Level 10))
Time Frame
Baseline, 6 months, 1 and 2 years post-operatively
Title
Return to Pre-injury Tegner Activity Level
Description
Proportion of patients returning to pre-injury levels, as measured by the Tegner Activity Scale (Values indicate level of activity from inactive (Level 0) to competitive level of activity (Level 10)).
Time Frame
1, 2 and 5 years post-operatively
Title
Cincinnati Occupational Rating Scale
Description
The Cincinnati Occupational Rating Scale assesses the level of work-related activities, including sitting, standing, walking, squatting, climbing, lifting and carrying weighted objects. The score ranges from 0 to 100, with a lower score representing more sedentary work-related activities.
Time Frame
Baseline, 3 and 6 months, 1, 2 and 5 years post-operatively
Title
Skin-to-Skin Operative Times
Description
Skin-to-skin operative times (in minutes) for each ACL reconstruction procedure
Time Frame
During surgery
Title
Radiographic (X-ray) Changes
Description
The analysis for the radiographic assessment data is currently ongoing, to provide a comparison of baseline, 2- and 5-year post-operative x-rays.
Time Frame
Baseline, 2 and 5 years post-operatively
Other Pre-specified Outcome Measures:
Title
Complications of the Surgical Procedure (See Adverse Events Section for Results of This Outcome)
Description
All complications/adverse events that occurred within the first two-years post-operatively. See Adverse Events section for results of this outcome.
Time Frame
2 years post-operatively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: A confirmed diagnosis of anterior cruciate ligament deficiency based on all of the following: History of a traumatic injury episode Physical examination findings of increased anterior translation of the tibia on the femur (Lachman test and/or anterior drawer test) A positive pivot shift test X-rays showing skeletal maturity (ie: tibial tubercle fused) and no fractures. (NB: Magnetic resonance imaging is not required) Age 14-50 years old Exclusion Criteria: Patients with combined ligament deficiencies (Posterior Cruciate, Medial and/or Lateral Collateral deficiency.) (NB: Grade 1 side to side differences (ie. < 5mm) on valgus, varus or posterior stress testing will not be considered exclusions) Intra-operative identification of International Cartilage Repair Society (ICRS) Grade 4 chondral lesion of > 1 cm ² [61] Previous ligament surgery on the affected or contralateral knees Cases involving litigation or Worker's Compensation Confirmed connective tissue disorder (ie: Ehlers-Danlos, Marfans) X-ray showing that tibial physis is not fused
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nicholas G Mohtadi, MD MSc FRCSC
Organizational Affiliation
University of Calgary Sport Medicine Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Calgary Sport Medicine Centre
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2N 1N4
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
9617395
Citation
Mohtadi N. Development and validation of the quality of life outcome measure (questionnaire) for chronic anterior cruciate ligament deficiency. Am J Sports Med. 1998 May-Jun;26(3):350-9. doi: 10.1177/03635465980260030201.
Results Reference
background
PubMed Identifier
21901700
Citation
Mohtadi NG, Chan DS, Dainty KN, Whelan DB. Patellar tendon versus hamstring tendon autograft for anterior cruciate ligament rupture in adults. Cochrane Database Syst Rev. 2011 Sep 7;2011(9):CD005960. doi: 10.1002/14651858.CD005960.pub2.
Results Reference
background
PubMed Identifier
25881568
Citation
Mohtadi N, Barber R, Chan D, Paolucci EO. Complications and Adverse Events of a Randomized Clinical Trial Comparing 3 Graft Types for ACL Reconstruction. Clin J Sport Med. 2016 May;26(3):182-9. doi: 10.1097/JSM.0000000000000202.
Results Reference
result
PubMed Identifier
25514139
Citation
Mohtadi N, Chan D, Barber R, Oddone Paolucci E. A Randomized Clinical Trial Comparing Patellar Tendon, Hamstring Tendon, and Double-Bundle ACL Reconstructions: Patient-Reported and Clinical Outcomes at a Minimal 2-Year Follow-up. Clin J Sport Med. 2015 Jul;25(4):321-31. doi: 10.1097/JSM.0000000000000165.
Results Reference
result
PubMed Identifier
26164058
Citation
Mohtadi N, Chan D, Barber R, Paolucci EO. Reruptures, Reinjuries, and Revisions at a Minimum 2-Year Follow-up: A Randomized Clinical Trial Comparing 3 Graft Types for ACL Reconstruction. Clin J Sport Med. 2016 Mar;26(2):96-107. doi: 10.1097/JSM.0000000000000209.
Results Reference
result
PubMed Identifier
31169571
Citation
Mohtadi NG, Chan DS. A Randomized Clinical Trial Comparing Patellar Tendon, Hamstring Tendon, and Double-Bundle ACL Reconstructions: Patient-Reported and Clinical Outcomes at 5-Year Follow-up. J Bone Joint Surg Am. 2019 Jun 5;101(11):949-960. doi: 10.2106/JBJS.18.01322.
Results Reference
result

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Comparison of Three Methods for Anterior Cruciate Ligament Reconstruction

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