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MZG Wire for Augmentation of ACL Reconstruction

Primary Purpose

Anterior Cruciate Ligament Rupture

Status
Not yet recruiting
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Magnesium Zinc Gadolinium alloy wire
Sponsored by
Chinese University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anterior Cruciate Ligament Rupture focused on measuring ACLR, MZG wire, Bone tendon interface healing

Eligibility Criteria

18 Years - 40 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age 18-40 Unilateral ACL tear for primary ACLR (Single bundle, Hamstring) confirmed clinically and radiologically. Exclusion Criteria: Concomitant multiple ligament injuries requiring additional surgical procedures, Preoperative radiographic signs of arthritis, Revision ACLR Femoral tunnel interference screws Contralateral knee with ACL deficiency or reconstruction Medical co-morbidities Long-term steroid intake Non-compliance to our rehabilitation protocol.

Sites / Locations

  • The Chinese University of Hong Kong

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

MZG Wire group

control group

Arm Description

Intervention: Magnesium Zinc Gadolinium (MZG) wire as braiding suture to braid the tendon graft.

2-0 vicryl suture as control, size and length matched MZG alloy wire

Outcomes

Primary Outcome Measures

Bone shell size
HR-pQCT (ExtremCT II, Scanco, Switzerland) will be used to measure the bone shell size at graft tunnel interface. The involved knees will be investigated. A total of 1344 axial slices with an image matrix of 2304 × 2304 were collected at a nominal isotropic voxel size of 60.7μm. The scan region was defined by the scout view image acquired in the sagittal plane.The total scanning length was 81.6mm which covered the tunnel from proximal tibia to distal femoral condyle (X-ray settings: 68kVp, 1470μA, 100ms integration time, 156mAs per stack (168 slices).Image segmentation will be performed to select the bone shell features at graft tunnel interfaces near femoral and tibial intra-articular apertures with standardized threshold values at a thickness of ~2.5 mm (40 slices). Geometric transformation will be performed to adjust for the variations in angle between scanning axis and tunnel axis by a cosine function.

Secondary Outcome Measures

International Knee Documentation Committee
Consists of 10 questions on symptoms and activity ranging from 0 to 100 where 100 implies perfect knee function.
Tegner activity score
This is an activity level scaled from 1 (low activity) to 10 (high activity).
Passive Knee laxity
To measure anterior-posterior knee laxity, the KT-1000 knee ligament arthrometer (MEDmetric Corp, San Diego, CA, USA) will be used. A manual force test will be applied until a 30lb sound signal is activated. Three trials will be performed. A side difference of 3 mm above is considered clinically relevant.
Isokinetic muscle strength
The dynamometer (Biodex System 4, Biodex Medical Systems Inc., New York, USA) will be used for measuring Isokinetic muscle strength in N. Subjects will perform a standardized warm-up exercise (5 min cycling) followed by the test. Concentric/concentric contractions of knee extension/flexion will be tested at 60°/s and 180°/s. Subjects will be seated on the dynamometer chair with their hips flexed to 85°.
Serum myokine evaluation
To evaluate the safety of MZG alloy wire with respect to inflammatory responses, 5 ml blood samples will be collected for C-reactive protein measurement using ELISA kit. Measurements of Ca, Mg, P, Cr, Urea, ALT, AST, TP, ALB, GLB will be taken to monitorpotential effect of the MZG alloy wire. The blood tests will be performed at baseline, day 1 post-op, 2 weeks, 6 weeks and 12 weeks post-op, since the degradation of MZG wire is faster based on our preclinical study results.
Single leg hop distance
The average of single leg hop distance in cm with three attempts will be measured during the single leg hop test.

Full Information

First Posted
July 31, 2023
Last Updated
August 7, 2023
Sponsor
Chinese University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT05983692
Brief Title
MZG Wire for Augmentation of ACL Reconstruction
Official Title
The Clinical Translation of a Biodegradable Magnesium Zinc Gadolinium Wire Developed for Augmentation of ACL Reconstruction, From Benchside to Bedside
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 2023 (Anticipated)
Primary Completion Date
September 2025 (Anticipated)
Study Completion Date
September 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Anterior Cruciate Ligament Reconstruction (ACLR) is the standard treatment of ACL injury. The most common grafts used for ACLR are autografts such as hamstring tendon graft. As this process requires the healing of two inhomogeneous tissues -bone with tendon, ACLR can be compromised by poor self-healing response. The use of biodegradable materials as implants to stimulate healing has been developed in orthopaedics for decades. In the ACLR model, our team and others reported that Mg based interference screw could consistently enhance ACLR by upregulating the expression of osteogenic and angiogenic factors experimentally. To improve on the potential insufficient mechanical strength of Mg-based screws in clinical applications, the investigators have developed a magnesium-zinc-gadolinium (MZG) alloy wire as a suture for braiding the tendon graft, following the standard procedure in our centre for the preparation of graft during ACLR. In a validated rabbit model, previous research found the MZG alloy wire showed good formability in material tests when being used as braiding suture, accompanied with the accelerated tunnel healing as shown by significantly more bone formation, and histologically with more regeneration of fibrocartilages at bone tendon healing interface. To further determine its efficacy and safety, MZG wire was tested in comparison with conventional suture in 16 goats as our pilot study. Radiological analysis of the femoral bone tunnel showed the bone volume fraction was significantly higher in MZG alloy wire group, with no significant difference seen in the safety tests. To determine whether the MZG alloy wire and its degradation over time after ACLR can promote graft healing and promote functional recovery in patients, the investigators propose to investigate the effect of using MZG alloy wire as a braiding suture in ACLR in a randomized controlled trial, with 30 patients in the intervention group using MZG alloy wire and 30 in the control group using conventional suture. As a direct measurement, High Resolution Peripheral Quantitative Computed Tomography (HR-pQCT) will be used to measure the microarchitecture in the bone shell tunnel. This novel use of MZG alloy wire as a braiding suture in ACLR, which is a standard procedure for the preparation of graft, that is not related to the fixation of the graft. This can incorporate the benefit of an Mg-based component for its degradation in vivo and release of osteogenic and angiogenic by-products, but without the risk of compromising the fixation of the tendon graft and without the need for additional steps during surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anterior Cruciate Ligament Rupture
Keywords
ACLR, MZG wire, Bone tendon interface healing

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
MZG Wire group
Arm Type
Experimental
Arm Description
Intervention: Magnesium Zinc Gadolinium (MZG) wire as braiding suture to braid the tendon graft.
Arm Title
control group
Arm Type
No Intervention
Arm Description
2-0 vicryl suture as control, size and length matched MZG alloy wire
Intervention Type
Device
Intervention Name(s)
Magnesium Zinc Gadolinium alloy wire
Intervention Description
MZG wire will be used as a braiding suture to braid tendon graft, which is a standard preparation of graft and is not related to fixation of the tendon graft
Primary Outcome Measure Information:
Title
Bone shell size
Description
HR-pQCT (ExtremCT II, Scanco, Switzerland) will be used to measure the bone shell size at graft tunnel interface. The involved knees will be investigated. A total of 1344 axial slices with an image matrix of 2304 × 2304 were collected at a nominal isotropic voxel size of 60.7μm. The scan region was defined by the scout view image acquired in the sagittal plane.The total scanning length was 81.6mm which covered the tunnel from proximal tibia to distal femoral condyle (X-ray settings: 68kVp, 1470μA, 100ms integration time, 156mAs per stack (168 slices).Image segmentation will be performed to select the bone shell features at graft tunnel interfaces near femoral and tibial intra-articular apertures with standardized threshold values at a thickness of ~2.5 mm (40 slices). Geometric transformation will be performed to adjust for the variations in angle between scanning axis and tunnel axis by a cosine function.
Time Frame
2 weeks and 3, 6, 12 and 24 months post-operation.
Secondary Outcome Measure Information:
Title
International Knee Documentation Committee
Description
Consists of 10 questions on symptoms and activity ranging from 0 to 100 where 100 implies perfect knee function.
Time Frame
Pre-operation, 2 weeks and 3, 6, 12 and 24 months post-operation.
Title
Tegner activity score
Description
This is an activity level scaled from 1 (low activity) to 10 (high activity).
Time Frame
Pre-operation, 2 weeks and 3, 6, 12 and 24 months post-operation.
Title
Passive Knee laxity
Description
To measure anterior-posterior knee laxity, the KT-1000 knee ligament arthrometer (MEDmetric Corp, San Diego, CA, USA) will be used. A manual force test will be applied until a 30lb sound signal is activated. Three trials will be performed. A side difference of 3 mm above is considered clinically relevant.
Time Frame
3, 6, 12 and 24 months post-operation.
Title
Isokinetic muscle strength
Description
The dynamometer (Biodex System 4, Biodex Medical Systems Inc., New York, USA) will be used for measuring Isokinetic muscle strength in N. Subjects will perform a standardized warm-up exercise (5 min cycling) followed by the test. Concentric/concentric contractions of knee extension/flexion will be tested at 60°/s and 180°/s. Subjects will be seated on the dynamometer chair with their hips flexed to 85°.
Time Frame
3, 6, 12 and 24 months post-operation
Title
Serum myokine evaluation
Description
To evaluate the safety of MZG alloy wire with respect to inflammatory responses, 5 ml blood samples will be collected for C-reactive protein measurement using ELISA kit. Measurements of Ca, Mg, P, Cr, Urea, ALT, AST, TP, ALB, GLB will be taken to monitorpotential effect of the MZG alloy wire. The blood tests will be performed at baseline, day 1 post-op, 2 weeks, 6 weeks and 12 weeks post-op, since the degradation of MZG wire is faster based on our preclinical study results.
Time Frame
Pre-operation, Day 1, 2 and 6 weeks and 3 months post-operation
Title
Single leg hop distance
Description
The average of single leg hop distance in cm with three attempts will be measured during the single leg hop test.
Time Frame
6, 12 and 24 months post-operation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18-40 Unilateral ACL tear for primary ACLR (Single bundle, Hamstring) confirmed clinically and radiologically. Exclusion Criteria: Concomitant multiple ligament injuries requiring additional surgical procedures, Preoperative radiographic signs of arthritis, Revision ACLR Femoral tunnel interference screws Contralateral knee with ACL deficiency or reconstruction Medical co-morbidities Long-term steroid intake Non-compliance to our rehabilitation protocol.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Michael Tim-Yun Ong
Phone
055699059
Email
michael.ong@cuhk.edu.hk
Facility Information:
Facility Name
The Chinese University of Hong Kong
City
Hong Kong
Country
Hong Kong

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Time Frame
starting 6 months after publication
IPD Sharing Access Criteria
Journal reviewers

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MZG Wire for Augmentation of ACL Reconstruction

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