A Prospective Randomized Pilot Study to Compare Open Versus Percutaneous Syndesmosis Repair of Unstable Ankle Fractures (ART)

February 25, 2019 updated by: David Sanders, Lawson Health Research Institute
This study evaluates fracture healing, anatomic reduction and return to functioning in patients with unstable Weber C type fractures of the ankle. Best outcomes are obtained when a good alignment of the ankle joint is maintained and natural function of the syndesmosis (space between the tibia and fibula bones) is restored. The syndesmosis and ankle joint is stabilized by a series of ligaments which are often damaged in Weber C type fractures. Current syndesmosis repair techniques traverse the tibia and fibula, but do not anatomically reconstruct the ligaments. The investigators will compare reconstruction of the unstable syndesmosis by open reduction and internal fixation using a syndesmosis screw coupled with anterior ligament (AiTFL) anatomic repair technique (ART) to percutaneous repair using a syndemosis screw only (SCREW). Radiographic, pain and functional outcome scores will be compared between the groups using validated outcome measures.

Study Overview

Detailed Description

High ankle fractures involve fracture of the fibula above the level of the syndesmosis (space between the tibia and fibula bones) that result from indirect mechanisms (e.g. pronation-external rotation (twisting) injuries. The method of injury is assumed to disrupt one or more of the syndesmotic ligaments, leading to instability of the ankle mortise . High ankle fractures comprise a significant proportion of ankle injuries (16 to 45 % of all ankle fractures patterns) . It is generally agreed that operative intervention of ankle injuries is indicated in cases of instability . However, recent advances in the understanding of the biomechanics of the ankle have given rise to particular areas of clinical uncertainty, including the treatment of unstable syndesmotic injuries and reliability of strictly radiographic assessment of ankle fractures .

The goal of operative treatment is to anatomically reduce the ankle mortise to permit syndesmosis ligament healing and restoration of the normal tibiofibular joint dynamics. Even 1 mm of displacement or lateral shift of the talus will affect ankle joint loading and lead to dysfunction and potentially degenerative joint changes. Accurate reduction of the syndesmosis and maintenance of this reduced position until the ligaments heal is crucial to ensure good outcome and to avoid long term arthritic changes in the tibiofibular joint .

If the ankle joint is unstable (too much sideways movement), the syndesmosis space between the two bones in the ankle (tibia and fibula) needs to be stabilized. One method to treat unstable syndesmosis injuries is making an incision to expose the ankle to provide direct visualization of fracture for anatomic reduction (alignment) and insertion of one or two syndesmosis screws to maintain the relationship of the fibula to the tibia. This is referred to as open reduction and internal fixation (ORIF).

Another method of repair is by closed reduction of the ankle joint and the use of one or two percutaneous syndesmosis screws only. That is, syndesmosis stabilization can be done percutaneously using intraoperative fluoroscopy to visualize the repair . Literature and standard practice support both of these methods.

The syndesmosis joint complex is composed of the anterior inferior tibiofibular ligament (AiTFL), the posterior inferior tibiofibular ligament (PiTFL) and the interosseous membrane (IOM). This complex is believed to permit ankle mortise stability and flexibility due to the elasticity of the ligaments, which allows the intermalleolar distance to change and facilitates tibial and fibular rotation. It also maintains the axis of balanced loading of the foot through the fibula. Adequate stability and anatomic restoration of the syndesmosis joint complex is vital to restoring normal tibiotalar contact forces in order to lessen the risk of posttraumatic arthritis.

Clinical studies have shown that anatomic reduction of the PiTFL provides a more accurate reduction of the ankle mortise than percutaneous reduction while ORIF fixation of the PiTFL has been shown on both biomechanical and clinical studies to provide greater stability than with syndesmotic screws alone .

However, due to the mechanism if injury, the AiTFL is the initial and may be the only lateral ligamentous stabilize structure compromised in syndesmotic injury. Kinematically, this ligament provides roughly half of the strength of the syndesmosis and acts as a vital primary restraint to excessive fibular displacement. The remainder of the stability is believed to come from bony restraints such as the posterior malleolus and the PiTFL . As such, direct reconstruction of the AiTFL component of the syndesmosis joint may accurately restore syndesmotic stability. Current syndesmosis repair techniques traverse the tibia and fibula (trans syndesmotic repair), but do not anatomically reconstruct the AiTFL.

Although it is known that an accurate reduction of the syndesmosis is essential to a good outcome, current treatments may have malreduction rates greater than 40% . In light of the existing models of syndesmosis injury, and the investigators' understanding of the importance of syndesmosis reduction, it may be that restoration of the AiTFL may potentially unlock a higher rate of anatomic reductions and positive outcomes.

Cadaveric and clinical studies have demonstrated that a flexible trans-osseous fixation technique may be viable and may improve ligamentous healing . However, current flexible techniques may not provide adequate stability and may not reduce the rate of malreduction compared to screw fixation.

The investigators recently conducted biomechanical studies in our lab using cadaveric ankles. The investigators compared whether a technique of syndesmosis repair concentrating on restoration of the AiTFL ligament (Anatomic repair technique or ART) provides a more anatomic reconstruction of the syndesmosis joint than rigid screw or posterior malleolus fixation.

The investigators' findings have demonstrated that our anatomic repair technique (ART) offers a repair which is sufficiently stable compared to screw fixation, with a lower incidence of malreduction as visualized on CT scan.

The investigator research suggests that ORIF repair of the AiTFL in addition to the stability provided by syndesmotic screw repair enhances syndesmosis stability substantially, as the AiTFL is a primary stabilizer to external rotation forces. In other words, fixing the anterior ligament may provide a better outcome and faster return to functioning.

Further in vivo testing is required to evaluate ART for repair of unstable syndesmosis injuries.

Study Type

Interventional

Enrollment (Actual)

50

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Ontario
      • London, Ontario, Canada, N6A4G5
        • London Health Sciences Centre

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. The subject is 18 years old or greater with a pre-operative diagnosis of a Weber C ankle fracture (supination-external rotation, pronation-external rotation, pronation-abduction patterns).
  2. The subject demonstrates lateral subluxation of the talus on x-ray or stress views (unstability).
  3. The lateral malleolus fracture if present begins at least 1.0 cm proximal to the syndesmosis.
  4. The subject has no history of previous ankle injury.
  5. The subject does not have an ipsilateral lower extremity injury that would impede results.
  6. The subject has no neuromuscular or neurosensory deficiency that would limit the ability to assess the operative procedure.

    -

Exclusion Criteria:

  1. The subject has a lateral malleolus fracture that begins less than 1.0 cm proximal to the syndesmosis.
  2. The subject has an open ankle fracture with a lateral wound. -

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Non-Randomized
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Screw

In the SCREW Group (standard surgery technique), surgical treatment will be by closed reduction utilizing intraoperative fluoroscopy to visualize the reduction and percutaneous syndesmosis screw insertion. Intraoperative fluoroscopic stress and non-stress views will be obtained as per standard of care.

'open reduction internal fixation (ORIF)

The study design is a prospective, randomized pilot clinical trial of the treatment of unstable syndesmosis injuries sustained with Weber C type fractures. Comparison will be made between two syndesmosis stabilization methods: 1) Percutaneous (closed) reduction using syndesmosis fixation by SCREW 2) Open reduction (ORIF) with ART repair of the anterior ligament and stabilization of the syndesmosis by use of a syndesmosis screw.
Active Comparator: Anatomic repair technique (ART)

In the ART group (study group) surgical treatment will be by open reduction and internal fixation. In order to stabilize the syndesmosis, direct visual anatomic alignment will be conducted and a syndesmotic screw inserted. In addition, fixation of the anterior ligament will be performed with use of a 2.7 to 4.0 mm suture anchor. Repair of the intact portion of the ligament will be made using a modified Mason -Allen repair. Intraoperative fluoroscopic stress and non-stress views will be obtained as per standard of care.

'open reduction internal fixation (ORIF)

The study design is a prospective, randomized pilot clinical trial of the treatment of unstable syndesmosis injuries sustained with Weber C type fractures. Comparison will be made between two syndesmosis stabilization methods: 1) Percutaneous (closed) reduction using syndesmosis fixation by SCREW 2) Open reduction (ORIF) with ART repair of the anterior ligament and stabilization of the syndesmosis by use of a syndesmosis screw.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
CT scan
Time Frame: 3 month
assessment of ankle alignment
3 month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Foot and Ankle Outcome Score (FAO),
Time Frame: 6 weeks, 3 , 6 , 12 months
Functional outcome assessment
6 weeks, 3 , 6 , 12 months
AOFAS Hindfoot Score
Time Frame: 6 weeks, 3 , 6 , 12 months
Functional outcome assessment
6 weeks, 3 , 6 , 12 months
Maryland Foot Score
Time Frame: 6 weeks, 3 , 6 , 12 months
Functional outcome assessment
6 weeks, 3 , 6 , 12 months
Radiographic healing
Time Frame: 6 weeks, 3 , 6 , 12 months
xray
6 weeks, 3 , 6 , 12 months
Complication- Infection
Time Frame: 6 weeks, 3 , 6 , 12 months
clinical and xray review of fracture documented
6 weeks, 3 , 6 , 12 months
Complication-Implant Failure
Time Frame: 6 weeks, 3 , 6 , 12 months
clinical and xray review of fracture documented
6 weeks, 3 , 6 , 12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: David Sanders, Western Univeristy/Lawson Health ResearcH Institute

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

August 1, 2013

Primary Completion (Actual)

September 1, 2016

Study Completion (Anticipated)

June 1, 2020

Study Registration Dates

First Submitted

September 17, 2014

First Submitted That Met QC Criteria

September 19, 2014

First Posted (Estimate)

September 22, 2014

Study Record Updates

Last Update Posted (Actual)

February 26, 2019

Last Update Submitted That Met QC Criteria

February 25, 2019

Last Verified

February 1, 2019

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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