Ankle Fractures Clinical Trial
Official title:
Operative Versus Non Operative Management Outcomes of Isolated Lateral Malleolar Weber B Ankle Fractures
Verified date | August 2018 |
Source | Cedars-Sinai Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The primary objective of this study is to determine the failure rate and difference in
clinical outcomes between operative and non operative treatment of patients with Weber B
lateral malleolus ankle fractures with medial clear space widening on gravity stress views.
All patients presenting will be treated non operatively, and compared to an observational
group comprised of patients with Weber B lateral malleolus ankle fractures without medial
clear space widening, for which the standard of care is non operative management.
Patients who decline non operative management and elect to undergo operative open reduction
internal fixation with plates and screws will comprise an operative observational cohort.
All patients will be followed for a total of 12 months from the time of injury. Clinical
outcomes will be based on radiographic monitoring for ankle mortise congruency, as well as
standardized SF-36 and AOFAS questionnaire scores.
Status | Not yet recruiting |
Enrollment | 200 |
Est. completion date | December 30, 2020 |
Est. primary completion date | July 18, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - 18-65 years old - able to provide informed consent Exclusion Criteria: - pregnancy - prisoners - psychiatric conditions that prevent ability to provide informed consent or present barriers to follow up - insulin dependent diabetics - patients with prior musculoskeletal issues affecting the same extremity - Patients cannot simultaneously be enrolled in any other studies. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Cedars-Sinai Medical Center |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | radiographic outcome of ankle congruency | measurement of medial clear space between medial malleolus and medial talar dome, measurement of tibiofibular overlap 1cm superior to the plafond, and measurement of superior clear space between the tibial plafond and the talar dome | 1 year | |
Secondary | functional outcome by American Orthopedic Foot and Ankle Score (AOFAS) scoring system | total score 0-100, with 100 being the maximum best score. (pain (0-40 points), function (0-50 points) and alignment (0-10 points) | 1 year | |
Secondary | additional functional outcome by Short Form Survey (SF-36) Score scoring system | 0 to 100 range, 100 being the best; subscores Physical functioning (0-10), Role limitations due to physical health (0-4), Role limitations due to emotional problems (0-3), Energy/fatigue (0-4)Emotional well-being (0-5), Social functioning (0-2), Pain (0-2), General Health 0-5 | 1 year | |
Secondary | functional outcome by American Orthopedic Foot and Ankle Score (AOFAS) - Pain score | none, mild occasional, moderate daily, severe and almost always present | 1 year | |
Secondary | functional outcome by American Orthopedic Foot and Ankle Score (AOFAS) - function - activity limitations, support requirements | no limitations and no support, no limitation of daily activities but limitation of recreational activities, limited daily and recreational activities, or severe limitation of daily and recreational activities | 1 year | |
Secondary | functional outcome by American Orthopedic Foot and Ankle Score (AOFAS) - alignment | good plantigrade, midfoot well aligned; fair plamtigrade, some degree of midfoot malalignment, poor with nonplantigrade foot, severe malalignment | 1 year |
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