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Clinical Trials/NCT04770818
NCT04770818
Unknown
Not Applicable

Lateral Ankle Ligament Reconstruction With InternalBrace™ Augmentation: A Prospective Randomized Study

Arthrex, Inc.3 sites in 1 country154 target enrollmentMarch 10, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Lateral Ankle Instability
Sponsor
Arthrex, Inc.
Enrollment
154
Locations
3
Primary Endpoint
Return to Work
Last Updated
5 years ago

Overview

Brief Summary

Lateral ankle ligament stabilization procedures are well described in the orthopaedic literature. Although success rates are high, the incidence of recurrent instability is well documented. In addition, with standard rehabilitation protocols, the timeline to return to sport and functional activities may be prolonged. The InternalBrace Ligament Augmentation Repair is a safe and reproducible technique using FiberTape® and BioComposite SwiveLock® as an augmentation to a Brostrom procedure. The InternalBrace Ligament Augmentation repair consists of a FiberTape bridge between two Knotless Swivelock anchors providing a protective reinforcement and allows the surgeon to repair lateral or medial ankle instability and the pain associated with it. This type of repair can be utilized in acute and chronic ankle sprains.

Detailed Description

It is hypothesized that use of InternalBrace Ligament Augmentation in addition to standard anatomic modified Brostrum repair allows for earlier return to pre-injury level compared to a standard Brostrum procedure. It is also secondarily hypothesized that intermediate and long term incidence of recurrent instability will be lower with use of internal brace augmentation of standard modified Brostrum lateral ankle ligament reconstruction.

Registry
clinicaltrials.gov
Start Date
March 10, 2016
End Date
March 10, 2023
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Return to Work

Time Frame: Subject is called every 2 weeks between 6-26 weeks post-op timepoint and asked when they returned to pre-injury level.

Subject self-assessment of time of return to pre-injury level.

Secondary Outcomes

  • Tegner Activity Score(Data collected at the following time points: Pre-operative, 6 weeks, 12 weeks and 26 weeks.)
  • Stress X-ray(Data will be collected at Pre-op and 1 year.)
  • Veterans Rand (VR-12)(Data collected at the following time points: Pre-operative, 6 weeks, 12 weeks, 26 weeks, 1 year, 2 years, 3 years, 4 years, 5 years)
  • Return to Sports(Data collected at the following time points: 6 weeks, 12 weeks and 26 weeks)
  • Karlsson and Peterson Scoring System(Data collected at the following time points: Pre-operative, 6 weeks, 12 weeks, 26 weeks, 1 year, 2 years, 3 years, 4 years, 5 years)
  • Range Of Motion(Data collected at the following time points: Pre-operative, 6 weeks, 12 weeks, 26 weeks and 1 year.)
  • Visual Analog Scale (VAS)(Data collected at the following time points: Pre-operative, 3 weeks, 6 weeks, 12 weeks, 26 weeks, 1 year, 2 years, 3 years, 4 years, 5 years)
  • Foot and Ankle Ability Measure (FAAM)(Data collected at the following time points: Pre-operative, 6 weeks, 12 weeks, 26 weeks, 1 year, 2 years, 3 years, 4 years, 5 years)

Study Sites (3)

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