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Ankle Fracture vs Ankle Fracture-Dislocation

Functional Outcome After Ankle Fractures and Ankle Fracture-Dislocations: A Prospective Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02198768
Enrollment
80
Registered
2014-07-24
Start date
2012-09-30
Completion date
2017-01-31
Last updated
2022-04-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ankle Fractures

Keywords

ankle fracture, ankle fracture-dislocation, prospective, observational

Brief summary

The purpose of this study is to compare outcomes of patients with an ankle fracture to those with ankle fracture-dislocations. We hypothesize that long-term clinical outcomes for patients sustaining ankle fracture dislocations are poorer than those without dislocation.

Detailed description

Orthopaedic literature has very limited data regarding outcomes following ankle fracture dislocations. Increased knowledge of the long-term consequences of these injuries could usher in changes to treatment paradigms, potentially resulting in improved outcomes. Thirty patients will be enrolled into two arms of this prospective study: isolated ankle fractures and ankle fracture dislocations. Patients will be followed through their operative and postoperative course and clinical and radiographic assessments will be analyzed. We plan to compare the clinical, radiographic, and functional outcomes of patients with ankle fractures to those with ankle fracture-dislocations. We also plan to identify factors that contribute to or predict poor clinical, functional, and/or radiographic outcomes in patients with ankle fractures and fracture-dislocations.

Interventions

None listed

Sponsors

Wake Forest University Health Sciences
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients who sustain an isolated bi-malleolar or trimalleolar ankle fracture or an ankle fracture-dislocation requiring open reduction internal fixation * Patients ages 18 and over * The subject is psychosocially, mentally, and physically able to understand and comply with the requirements of the study * Open and closed fractures (excluding Gustilo grade 3) * English must be patient's primary language

Exclusion criteria

* Previous injury or significant osteoarthritis to the affected ankle * Current ipsilateral or contralateral lower extremity injury with the exception of a contralateral ankle fracture or fracture-dislocation * Retained hardware from a previous injury at or around the tibia-talar joint of the affected extremity * Patients under the age of 18 * History of inflammatory arthropathy * Traumatic Brain Injury or Spinal Cord Injury preventing weightbearing on the lower extremities * The subject has another concurrent physical or mental condition that is likely to affect compliance with the study requirements * Patients with Gustilo grade 3B and 3C open fractures

Design outcomes

Primary

MeasureTime frameDescription
Change in Functional Outcome6, 12, and 24 monthsClinical and functional outcomes will be measured using the Foot and Ankle Ability Measure (FAAM) and the Short Form Musculoskeletal Functional Assessment (SMFA). Radiographic analysis will be performed to determine nonunion, malunion, joint space incongruity, hardware failure/loosening, and/or severity of osteoarthritis. The Van Dijk grading scale will be used for radiographic assessment.

Secondary

MeasureTime frameDescription
Radiographic Outcome24 monthRadiographic analysis will be performed to determine nonunion, malunion, joint space incongruity, hardware failure/loosening, and/or severity of osteoarthritis. The Van Dijk grading scale will be used for radiographic assessment.

Other

MeasureTime frameDescription
Additional surgical procedures2 yearsDocumentation of any additional surgical procedures conducted on the affected ankle. Any surgical procedure will be noted. These may include debridement for infection or dehiscence, revision for hardware failure, arthroscopy, ankle arthrodesis, or cartilage restoration procedures.
Postoperative Complications2 yearsPostoperative complications will be documented and analyzed to determine if there are significant differences between the two groups. These will include infection requiring antibiotics or debridement, hardware failure, nerve or vascular injury, deep venous thrombosis, or revision surgery.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026