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Acute Anterior Cruciate Ligament Rupture; RecOnsTruction Or Repair? (ROTOR)

Primary Purpose

Anterior Cruciate Ligament Injury

Status
Active
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
ACL Repair
ACL reconstruction
Sponsored by
Orthopedisch Centrum Oost Nederland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Anterior Cruciate Ligament Injury focused on measuring anterior cruciate ligament rupture, autograft, reconstruction, orthopedic surgery, dynamic intraligament stabilization

Eligibility Criteria

18 Years - 30 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Sportive, active patient (Tegner score =/>5)
  • Age above 18 untill 30 years at time of inclusion
  • Primary rupture of the anterior cruciate ligament, evidence by history (acute trauma, clicking sensation, swelling within a few hours, instability) and physical examination (positive Lachman, anterior drawer test and/or Pivot shift)
  • Primary rupture indicated by MRI
  • No associated ligamentuous disorde of the knee, evidenced by history, physical examination, x-ray or MRI)
  • Time span between anterior cruciate ligament rupture and operation no longer than 21 days
  • Willingness to comply to advised rehabilitation protocol supervised by (NFVS registrated) sports physiotherapist

Exclusion Criteria:

  • Infection
  • Known hypersensitive response for materials used (Cobalt, chroom, nickel)
  • Serieus pre-existing malaligment of leg indicated for surgery
  • Tendency for excessive scar tisseu formation, such as arthrofibrosis
  • History of previous surgery on leg indicated for surgery
  • History of removal of tendon on leg indicated for surgery
  • Muscular, neurological or vascular disorders negatively affecting healing or rehabilitation
  • Cartilage injury requiring (some kind of) cartilage repair surgery (such as microfracture or cell therapy)
  • Arthrosis more dan ICRS grade 2 evidenced by x-ray
  • Long(er) term use of relevant medication, such as prednisolon or cytostatica
  • Pregnancy
  • Know osteoporosis

Sites / Locations

  • Orthopedisch Centrum Oost Nederland /ZGT

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

ACL Reconstruction

ACL Repair

Arm Description

Primary reconstructive surgery of ACL with hamstring autograft (All-inside, Arthrex, Napels, Florida, USA)

Primary augmented suture of ACL using Dynamic Intraligament Stabilization (DIS; Mathys Medical Bettlach, Switzerland)

Outcomes

Primary Outcome Measures

IKDC 2000 subjective knee evaluation form
questionniare/self-reported functional limitations in activitities of daily living and/or sports activities

Secondary Outcome Measures

IKDC 2000 subjective knee evaluation form
questionnaire/self-reported functional limitations in activitities of daily living and/or sports
IKDC 2000 objective knee evaluation form
knee physical examination form / clinimetrics
Knee Injury and Osteoarthritis Outcome Score (KOOS)
questionnaire designed to assess short and long term patient-related ouctome following knee injury on pain, symptoms, activities of daily living, sport and recreation, knee-related quality of life
Tegner Activity Level Scale
Rating scale to determine the type and intensity of sports/activities
Instrumented anteroposterior laxity
LSI jump-force testing
leg symmetry index for jump tests as well as isokinetic quadriceps and hamstring force tests

Full Information

First Posted
December 1, 2014
Last Updated
June 22, 2020
Sponsor
Orthopedisch Centrum Oost Nederland
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1. Study Identification

Unique Protocol Identification Number
NCT02310854
Brief Title
Acute Anterior Cruciate Ligament Rupture; RecOnsTruction Or Repair?
Acronym
ROTOR
Official Title
Acute Anterior Cruciate Ligament Rupture; RecOnsTruction Or Repair?
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 2014 (Actual)
Primary Completion Date
December 2016 (Actual)
Study Completion Date
November 2029 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Orthopedisch Centrum Oost Nederland

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To investigate the hypothesis that suture repair of a ruptured vkb, combined with a dynamic intraligamentary stabilization and microfracture of the femoral notch, results in at least equal effectiveness compared with an ACL reconstruction using autologous hamstring in terms of functional recovery one year postoperatively in terms of a patient self-reported outcome related to be able to conduct daily and sporting activities. Secondary, the evaluation of clinical outcomes, self-reported by the patient outcomes, osteoarthritis, rehabilitation time required for return to daily and sporting activities and levels of sporting activity which has returned in patients with status after an ACL rupture and suture repair augmented with a dynamic intraligamentary microfracture and stabilization of the femoral notch in comparison with an anterior cruciate ligament reconstruction with the ipsilateral hamstring graft.
Detailed Description
Background of the study: An anterior cruciate ligament rupture is a serious injury to the knee with high probability of the occurrence of dynamic instability, accompanying lesions and early post-traumatic arthrosis. Despite conservative treatment through rehabilitation or ACL reconstruction surgery not all patients do return to their previous activity levels. Moreover degenerative changes, especially early posttraumatic arthrosis, are not counteracted. In order to optimize the clinical results after ACL surgery, a renewed interest has emerged in healing the patient's own ruptured ACL after attaching. Literature suggests that with the current innovations in surgical repair techniques of (natural) healing of a ruptured ACL may result in similar clinical outcomes in comparison to the gold standard, the ACL reconstruction. In addition, it may even reduce degenerative changes occur in relation to the gold standard. Moreover, the return to daily activities and sports level seems significantly faster than after ACL reconstruction. The hypothesis is that a suture (suture repair) of a ruptured ACL, combined with a dynamic intraligamentary stabilization, as well as microfracture of the femoral notch, passes, at least equal efficacy in comparison with an anterior cruciate ligament reconstruction using autologous hamstrings in terms of functional recovery 1 years postoperatively. The DIS bonding technique will be applied in the current study to surgically repair (suture) the ruptured ACL. DIS is an abbreviation and stands for intraligamentary dynamic stabilization (DIS). DIS has been used in humans and seems to provide a high patient satisfaction, favorable clinical and radiological results. However, to our knowledge, to date, no randomized comparative study has been conducted yet in which the DIS technique is compared with the gold standard, the ACL reconstruction. Objective of the study: Primary goal: Investigate the hypothesis that suture repair of a ruptured vkb, combined with a dynamic intraligamentary stabilization and microfracture of the femoral notch, results in at least equal effectiveness compared with an ACL reconstruction using autologous hamstring in terms of functional recovery one year postoperatively in terms of a patient self-reported outcome related to be able to conduct daily and sporting activities. Secondary objective: Evaluation of clinical outcomes, self-reported by the patient outcomes, osteoarthritis, rehabilitation time required for return to daily and sporting activities and levels of sporting activity which has returned in patients with status after an ACL rupture and suture repair augmented with a dynamic intraligamentary microfracture and stabilization of the femoral notch in comparison with an anterior cruciate ligament reconstruction with the ipsilateral hamstring graft. Study design: This study is a single center stratified block randomized controlled trial. Patients with ACL rupture, confirmed by an orthopedic surgeon based on the outpatient history and radiographic images, will be randomized into an experimental ('repair' / DIS) group after inclusion and a control (reconstruction, regular care) group. Patients will be stratified on the level of sport/physical active practice, on the basis of the Tegner score. The Tegner score is an evaluative and inventory questionnaire on which the patient indicates the gravity of his work and/or sports activities. A higher score is associated with a higher level of physical strain/activity . On the basis of the Tegner score patients will be stratified into a 'moderate' physically active stratum (group Tegner score 5-6-7) and 'highly' physically active stratum (group Tegner score 8 -9-10). Stratification based on the degree of physical activity is considered to be important because the extent and severity of physical activity/strain in daily life poses a potential (difference) in risk of re-rupture between the two study arms. In order to minimize potential differences in 'exposure' or 'risk of re-rupture' between the two study groups stratification is relevant.Measurements take place at baseline, peri-operative / immediately after surgery, 6 weeks, 3,6,9 months and 1, 2, 5 and 10 years postoperatively. Study population: (Physically) active patients from 18 untill 30 years, who has visited the outpatient clinic of the orthopedic surgeon because of a knee injury resulting in a ACL rupture, for whom surgery indication for an ACL reconstruction exists and who can be operated on within three weeks after the onset of the ACL rupture. Intervention: n=48 patients will participate in the current study. Patients will be assigned to a suture repair of the ruptured vkb complemented by a dynamic intraligamentary stabilization (DIS) and microfracture of the femoral notch or the gold standard, a ACL reconstruction. Primary study parameters/outcome of the study: Self-reported functional outcome at one-year follow post surgery measured by the IKDC 2000 subjective scale. Secundary study parameters/outcome of the study (if applicable): Secondaire eindpunten: Self-reported functional outcome at one-year follow post surgery measured by the IKDC 2000 subjective scale 6 weeks, 3,6 and 9 months, 2,5 and 10 years post surgery, self-reported disabilities (KOOS), level of physical activity (Tegner), satisfaction (VAS) as well as IKDC physical examination (clinimetretrics) 6 weeks, 3, 6 en 9 months, 1, 2, 5 and 10 years post surgery; instrumented anteroposterior laxity, leg symmetry index for jump tests as well as isokinetic quadriceps en hamstrings force 6 en 9 months, 1, 2, 5 en 10 years after surgery; radiologic signs of arthrosis 1,2 5 and 10 years post surgery; reruptures of the ACL within 10 years post surgery, classification rupture pattern peroperative.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anterior Cruciate Ligament Injury
Keywords
anterior cruciate ligament rupture, autograft, reconstruction, orthopedic surgery, dynamic intraligament stabilization

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
48 (Actual)

8. Arms, Groups, and Interventions

Arm Title
ACL Reconstruction
Arm Type
Active Comparator
Arm Description
Primary reconstructive surgery of ACL with hamstring autograft (All-inside, Arthrex, Napels, Florida, USA)
Arm Title
ACL Repair
Arm Type
Experimental
Arm Description
Primary augmented suture of ACL using Dynamic Intraligament Stabilization (DIS; Mathys Medical Bettlach, Switzerland)
Intervention Type
Procedure
Intervention Name(s)
ACL Repair
Other Intervention Name(s)
Dynamic Intraligament Stabilization (DIS), Augmented suture
Intervention Description
augmented suture of acute ACL rupture (<3 weeks after injury)
Intervention Type
Procedure
Intervention Name(s)
ACL reconstruction
Other Intervention Name(s)
Primary ACL reconstruction, Autograft hamstring, All-inside
Intervention Description
reconstruction hamstring autograft
Primary Outcome Measure Information:
Title
IKDC 2000 subjective knee evaluation form
Description
questionniare/self-reported functional limitations in activitities of daily living and/or sports activities
Time Frame
baseline, 12 months post surgery
Secondary Outcome Measure Information:
Title
IKDC 2000 subjective knee evaluation form
Description
questionnaire/self-reported functional limitations in activitities of daily living and/or sports
Time Frame
baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery
Title
IKDC 2000 objective knee evaluation form
Description
knee physical examination form / clinimetrics
Time Frame
baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery
Title
Knee Injury and Osteoarthritis Outcome Score (KOOS)
Description
questionnaire designed to assess short and long term patient-related ouctome following knee injury on pain, symptoms, activities of daily living, sport and recreation, knee-related quality of life
Time Frame
baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery
Title
Tegner Activity Level Scale
Description
Rating scale to determine the type and intensity of sports/activities
Time Frame
baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery
Title
Instrumented anteroposterior laxity
Time Frame
baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery
Title
LSI jump-force testing
Description
leg symmetry index for jump tests as well as isokinetic quadriceps and hamstring force tests
Time Frame
6-9-12 months, 2-5-10 years post surgery
Other Pre-specified Outcome Measures:
Title
Reinjuries
Description
reinjuries or reruptures of the knee
Time Frame
up till 10 years post surgery
Title
workability
Description
questionnaire to assess the patient's workability due to knee injury/knee surgery in order to be able to make an estimation of costs benefits between study arms
Time Frame
baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery
Title
Classification of type of rupture of the ACL
Description
The surgeon's opinion regarding the classification of the type of rupture of the ACL peroperative.
Time Frame
during surgery
Title
Complications associated with knee surgery and/or rehabilitation
Description
The complications that occur as a result of the ACL surgery and/or rehabilitation in time.
Time Frame
baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery
Title
x-ray knee
Description
x-ray will be taken of the knee in order to be able to determine the degree of arthrosis
Time Frame
5 and 10 years post surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Sportive, active patient (Tegner score =/>5) Age above 18 untill 30 years at time of inclusion Primary rupture of the anterior cruciate ligament, evidence by history (acute trauma, clicking sensation, swelling within a few hours, instability) and physical examination (positive Lachman, anterior drawer test and/or Pivot shift) Primary rupture indicated by MRI No associated ligamentuous disorde of the knee, evidenced by history, physical examination, x-ray or MRI) Time span between anterior cruciate ligament rupture and operation no longer than 21 days Willingness to comply to advised rehabilitation protocol supervised by (NFVS registrated) sports physiotherapist Exclusion Criteria: Infection Known hypersensitive response for materials used (Cobalt, chroom, nickel) Serieus pre-existing malaligment of leg indicated for surgery Tendency for excessive scar tisseu formation, such as arthrofibrosis History of previous surgery on leg indicated for surgery History of removal of tendon on leg indicated for surgery Muscular, neurological or vascular disorders negatively affecting healing or rehabilitation Cartilage injury requiring (some kind of) cartilage repair surgery (such as microfracture or cell therapy) Arthrosis more dan ICRS grade 2 evidenced by x-ray Long(er) term use of relevant medication, such as prednisolon or cytostatica Pregnancy Know osteoporosis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
R.A.G Hoogeslag, MD
Organizational Affiliation
OCON
Official's Role
Principal Investigator
Facility Information:
Facility Name
Orthopedisch Centrum Oost Nederland /ZGT
City
Hengelo
ZIP/Postal Code
7555
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
to be determined yet
Citations:
PubMed Identifier
30822124
Citation
Hoogeslag RAG, Brouwer RW, Boer BC, de Vries AJ, Huis In 't Veld R. Acute Anterior Cruciate Ligament Rupture: Repair or Reconstruction? Two-Year Results of a Randomized Controlled Clinical Trial. Am J Sports Med. 2019 Mar;47(3):567-577. doi: 10.1177/0363546519825878.
Results Reference
derived
PubMed Identifier
29678170
Citation
Boer BC, Hoogeslag RAG, Brouwer RW, Demmer A, Huis In 't Veld RMHA. Self-reported functional recovery after reconstruction versus repair in acute anterior cruciate ligament rupture (ROTOR): a randomized controlled clinical trial. BMC Musculoskelet Disord. 2018 Apr 20;19(1):127. doi: 10.1186/s12891-018-2028-4.
Results Reference
derived

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Acute Anterior Cruciate Ligament Rupture; RecOnsTruction Or Repair?

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