Syndesmosis Ankle Study
Weight-Bearing Timing and Outcomes After Surgical Suture Button Repair of the Distal Tibiofibular Syndesmosis
A debate regarding ankle fracture fixation centers on time to weight bearing. Recent literature has supported immediate weight bearing in surgically stabilized ankle fractures. However, significant variation among orthopaedic surgeons persists, and weight bearing recommendations change when there is a syndesmotic disruption. There is very little literature on time to weight bearing, with most available series casting/immobilizing these injuries for 6 weeks after fixation. There is very little data examining post-operative weight bearing after syndesmotic stabilization, and the majority centers on screw fixation. The minimum time to weight bearing after an ankle fracture with syndesmotic fixation in the literature is 4 weeks, with most focusing on 6 to 12 weeks. Based on biomechanical data regarding suture button techniques, the investigators hypothesize that patients undergoing ankle fracture fixation plus suture button fixation of their syndesmotic disruption will be able to safely bear weight early (2 weeks) after surgery. The investigator's null hypothesis is that there will be no difference between early weight bearing (2 weeks), and late weight bearing (6 weeks) in terms of outcome, hardware failure, loss of reduction, and return to work.
Adult patients who have an ankle fracture with suspected syndesmotic disruption, requiring a suture button fixation operative intervention will be randomized into early (2 weeks post-surgically) weight-bearing status or delayed weight-bearing status (non-weight-bearing for 6 weeks following fixation).
Primary objective: Maintenance of ankle reduction at 1 year follow-up (measured by comparing immediate post-op CT and 1 year time-point CT).
Secondary Objectives: Pain scores, surgical experience, work productivity and activity impairment , AAOS foot and ankle scores (2w, 6w, 12w, 6m, 1y), use of assistive devices, range of motion, physical therapy requirement/length of use/compliance, post-operative protocol compliance, post-operative complications (wound healing, infection, implant failure, fracture healing).
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Missouri
-
Columbia, Missouri, United States, 65212
- Vicki Jones
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 18 years of age or older
- Ankle fracture with suspected syndesmotic disruption that would likely be treated with suture button fixation operative intervention
- Ability to ambulate preoperatively
Exclusion Criteria:
- Younger than 18
- Length unstable syndesmotic injury (i.e. Maisonneuve)
- Neuropathic diabetics
- 325 pounds or more
- Prisoner
- Pregnant or lactating
- End stage renal disease
- Inability to follow commands (dementia, TBI, etc.)
- Polytrauma patients
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Early Weight-Bearing
Being directed to bear weight on the affected ankle two weeks from suture button fixation for syndesmotic disruption
|
Being directed to bear weight on the affected ankle two weeks from suture button fixation for syndesmotic disruption
|
|
Active Comparator: Delayed/Late Weight-Bearing
Being directed to bear weight on the affected ankle six weeks from suture button fixation for syndesmotic disruption
|
Being directed to bear weight on the affected ankle six weeks from suture button fixation for syndesmotic disruption
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Measure of the syndesmotic change
Time Frame: 1 year
|
Determined by comparing the 1-year, post-operative CT scan to the immediate post-operative CT scan of the injured ankle
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain scores
Time Frame: 2 weeks to 1 year
|
Measured on a 0-10 scale by VAS or PROMIS patient reported outcome forms
|
2 weeks to 1 year
|
|
Surgical Experience (SSQ-8)
Time Frame: Day 0
|
The SSQ-8 (Surgical Satisfaction Score) is a patient administered 8-item survey designed to asses satisfaction after a surgical procedure.
Answers are then measured on a scale of 1 to 5 or 6, with 1 being the best outcome score.
|
Day 0
|
|
Work productivity and activity impairment (WPAI)
Time Frame: 6 weeks to 1 year
|
The Work Productivity and Activity Impairment (WPAI) questionnaire is a self-administered instrument used to assess the impact of disease on productivity.
The sum of specific health problem impairment and impairment due to other health reasons is equal to impairment due to all health reasons.
WPAI outcomes are expressed as impairment percentages, with higher numbers indicating greater impairment and less productivity, i.e., worse outcomes.
|
6 weeks to 1 year
|
|
Foot and ankle outcomes (AAOS)
Time Frame: 2 weeks to 1 year
|
The AAOS foot and ankle questionnaire is a patient-administrated 25-item survey specifically developed for foot and ankle-related disability.
The questionnaire is divided into two scales, the Foot and Ankle Core scale, comprised of 20 questions and the Shoe Comfort Scale with five questions.
The questions themselves are distributed amongst five different categories: Pain (9 items), function (6 items), stiffness and swelling (2 items), giving way (3 items) and shoe comfort (5 items).
Answers are then measured on a scale of 1 to 5 or 6, with1 being the best outcome score.
|
2 weeks to 1 year
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Kyle Schweser, MD, University of Missouri Health System, Department of Orthopaedic Surgery
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2014428
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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