A Comparison of Stainless Steel and Bioabsorbable Screw Fixation of Lisfranc Foot Injuries (Lisfranc)
Primary Purpose
Unstable Lisfranc Fracture-dislocations of the Midfoot
Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Steel screw fixation of Lisfranc fracture-dislocation.
Absorbable screw fixation of Lisfranc fracture-dislocations.
Sponsored by
About this trial
This is an interventional treatment trial for Unstable Lisfranc Fracture-dislocations of the Midfoot focused on measuring Unstable, Lisfranc, fracture, dislocation, midfoot
Eligibility Criteria
Inclusion Criteria:
- Subjects will be adults of any gender or race.
- The underlying diagnosis will be a Lisfranc foot injury.
- The indication for fixing the Lisfranc ligaments is abnormal separation of the middle part of the foot from each other.
- Subjects will have received either a steel or absorbable screw to fix the Lisfranc ligaments.
Exclusion Criteria:
- Subjects must not have intact or normal Lisfranc ligaments in the foot.
Sites / Locations
- Riddle Memorial Hospital
- Nazareth Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Steel screw fixation
Bioabsorbable screw fixation
Arm Description
Outcomes
Primary Outcome Measures
Return to pre-injury level of function.
Secondary Outcome Measures
Restoration of normal midfoot alignment and stability.
Full Information
NCT ID
NCT00985023
First Posted
September 23, 2009
Last Updated
January 13, 2017
Sponsor
Rothman Institute Orthopaedics
1. Study Identification
Unique Protocol Identification Number
NCT00985023
Brief Title
A Comparison of Stainless Steel and Bioabsorbable Screw Fixation of Lisfranc Foot Injuries
Acronym
Lisfranc
Official Title
A Randomized, Prospective Comparison of Stainless Steel and Bioabsorbable Screw Fixation of Lisfranc Foot Injuries
Study Type
Interventional
2. Study Status
Record Verification Date
January 2017
Overall Recruitment Status
Completed
Study Start Date
August 2008 (undefined)
Primary Completion Date
August 2016 (Actual)
Study Completion Date
August 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rothman Institute Orthopaedics
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The Lisfranc ligaments are a group of ligaments that connect the bones of the middle portion of the foot to each other. The Lisfranc ligaments allow for a normal and stable range of motion and shape to the foot. In certain foot fractures where the Lisfranc ligaments are damaged, the constraint and stability it had given to the middle of the foot is lost. Attempted activity at the foot will result in pain and abnormal motion. If injury to the Lisfranc ligaments is left untreated, the eventual end result is foot arthritis and deformity.
The current standard orthopaedic treatment of foot fractures with Lisfranc ligament injuries is surgery. The foot fractures are fixed with metal screws. The Lisfranc ligaments are fixed by compressing the space between the middle bones of the foot with steel screws. These screws allow for ligament healing. As the ligaments heal, the patient should not resume activity with the fixed foot too soon as the screw may break. Upon breakage, the ligament repair may fail and the screw is now difficult to surgically remove. Regardless of breakage, a second surgical procedure is often recommended to remove the steel screw 6 months after foot surgery. This allows for a complete return of normal foot range of motion, but at the cost of a second surgical procedure.
The investigators hypothesize that absorbable screw fixation of the Lisfranc ligaments does not yield significant differences in postoperative foot stability, ligament function, and symptoms when compared to steel screw fixation. In addition, absorbable screw fixation of the Lisfranc ligaments offers the advantage that a second surgical procedure to remove the screw is not necessary.
Detailed Description
The Lisfranc ligaments are a group of ligaments that connect the bones of the middle portion of the foot to each other. The Lisfranc ligaments allow for a normal and stable range of motion and shape to the foot.
In certain foot fractures, the Lisfranc ligaments are damaged. When the Lisfranc ligaments are disrupted, the constraint and stability it had given to the middle of the foot is lost. Attempted activity at the foot will result in pain and abnormal motion. If injury to the Lisfranc ligaments is left untreated, the eventual end result is foot arthritis and deformity.
The current standard orthopaedic treatment of foot fractures with Lisfranc ligament injuries is surgery. The foot fractures are fixed with metal screws. The Lisfranc ligaments are fixed by compressing the space between the middle bones of the foot with steel screws. These screws allow for ligament healing. As the ligaments heal, the patient should not resume activity with the fixed foot too soon as the screw may break. Upon breakage, the ligament repair may fail and the screw is now difficult to surgically remove. Regardless of breakage, a second surgical procedure is often recommended to remove the steel screw 6 months after foot surgery. This allows for a complete return of normal foot range of motion, but at the cost of a second surgical procedure.
The use of materials that can be absorbed by the human body to fix the Lisfranc ligaments has only been studied in 1 paper. One such material is the Smart Screw (Bionx, Blue Bell, Pennsylvania) which is approved by the Food and Drug Administration (F.D.A.) and made of polylevolactic acid (PLA). Absorbable screws could be ideal for the treatment of Lisfranc ligament injuries. They can provide a mechanical scaffold to allow for ligament healing. They are absorbable which eliminates the need for a second surgery to remove a screw. They can be used for foot injuries where the rate of healing and thus absorption is rapid. Although, absorbable implants are weaker than metal implants, the absorbable screw can be protected from breaking by restricting weight bearing after surgery. If the absorbable screw does break, there is no need to remove the fragments in the foot bones as they are absorbable.
Comparing the long-term results of fixing the Lisfranc ligaments with either a steel or absorbable screw is important as there are no studies on the subject to date. There is only 1 published study regarding absorbable screws to fix the Lisfranc ligaments. The purpose of this study is to compare the outcome of steel and absorbable screw fixation of the Lisfranc ligaments in foot injuries in two surgeons' practice.
We hypothesize that absorbable screw fixation of the Lisfranc ligaments does not yield significant differences in postoperative foot stability, ligament function, and symptoms when compared to steel screw fixation. In addition, absorbable screw fixation of the Lisfranc ligaments offers the advantage that a second surgical procedure to remove the screw is not necessary.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Unstable Lisfranc Fracture-dislocations of the Midfoot
Keywords
Unstable, Lisfranc, fracture, dislocation, midfoot
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
50 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Steel screw fixation
Arm Type
Active Comparator
Arm Title
Bioabsorbable screw fixation
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
Steel screw fixation of Lisfranc fracture-dislocation.
Other Intervention Name(s)
Steel screw
Intervention Description
Stainless steel screw fixation of unstable Lisfranc fracture-dislocations of the midfoot.
Intervention Type
Procedure
Intervention Name(s)
Absorbable screw fixation of Lisfranc fracture-dislocations.
Other Intervention Name(s)
Smart Screw
Intervention Description
Bioabsorbable (poly-levo-lactic acid) screw fixation of unstable Lisfranc fracture-dislocations of the midfoot.
Primary Outcome Measure Information:
Title
Return to pre-injury level of function.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Restoration of normal midfoot alignment and stability.
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Subjects will be adults of any gender or race.
The underlying diagnosis will be a Lisfranc foot injury.
The indication for fixing the Lisfranc ligaments is abnormal separation of the middle part of the foot from each other.
Subjects will have received either a steel or absorbable screw to fix the Lisfranc ligaments.
Exclusion Criteria:
Subjects must not have intact or normal Lisfranc ligaments in the foot.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jamal Ahmad, M.D.
Organizational Affiliation
Rothman Institute Orthopaedics
Official's Role
Principal Investigator
Facility Information:
Facility Name
Riddle Memorial Hospital
City
Media
State/Province
Pennsylvania
ZIP/Postal Code
19063
Country
United States
Facility Name
Nazareth Hospital
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19152
Country
United States
12. IPD Sharing Statement
Learn more about this trial
A Comparison of Stainless Steel and Bioabsorbable Screw Fixation of Lisfranc Foot Injuries
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