Ankle Injuries Clinical Trial
Official title:
A Prospective Randomized Multi-Centre Study to Compare Operative Versus Non Operative Functional Treatment in Patients With Unstable Isolated Fibula Fractures
Verified date | September 2016 |
Source | Lawson Health Research Institute |
Contact | n/a |
Is FDA regulated | No |
Health authority | Canada: Health Canada |
Study type | Interventional |
The purpose of the study is to compare functional outcomes and recovery following surgical
and non surgical treatment of potentially unstable , isolated fibula fractures. Secondary
objectives are to compare the re-operation rate, time to union and complications between the
two treatment groups.
The primary research questions:
1. Does surgery provide a better functional outcome compared to non operative treatment of
undisplaced, unstable fractures?
2. Do patients with these fractures return to activities faster after operative or non
operative treatment?
3. Are complications more common with operative or non operative care?
Status | Completed |
Enrollment | 80 |
Est. completion date | August 2010 |
Est. primary completion date | August 2010 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: 1. Skeletally mature male or female < 65 years of age 2. Unstable ankle on stress exam: medial clear space ³ 5 mm: no Mortise shift on static radiographs 3. Unilateral Weber B fibular fractures 4. Closed fracture 5. Provision of informed consent - Exclusion Criteria: 1. Fractures not amenable to surgical treatment 2. Pathologic fracture 3. Associated injuries to the foot, ankle, tibia, or knee 4. Associated medial malleolus fracture 5. Surgical delay of >2 weeks from time of injury 6. Previous fracture or retained hardware in the affected limb 7. Associated neurovascular injury or deficit in the affected limb 8. Systemic diseases including diabetes, multiple sclerosis, Parkinson's disease, and other disorders which might affect peripheral sensorimotor function - |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Canada | LOndon Health Sciences cEntre- Victoria Hospital | LOndon | Ontario |
Lead Sponsor | Collaborator |
---|---|
Lawson Health Research Institute |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Primary outcome: comparison of physical functioning score on SF36 | enrolment, 6 weeks, 3,6 12 months | Yes | |
Secondary | Secondary objectives are to compare the re-operation rate between operative and non-operative treatment and to compare the time to union, rates of nonunion and complications such as infection between the two groups. | Number of participants with complications or adverse events that ae related to treatment | enrolment, 6 weeks, 3,6,12 months | Yes |
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