Femur Fractures Clinical Trial
Official title:
Isolated Locked Compression Plating Versus Cable Plating and Strut Allografts With Cerclage Wiring for Vancouver B1 Periprosthetic Femoral Fractures: A Randomized Controlled Trial
NCT number | NCT01354535 |
Other study ID # | 13052011 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | February 2013 |
Est. completion date | June 2023 |
The purpose of this study is to compare two different but standard treatments for the fixation of Vancouver B1 periprosthetic. The investigators aim to compare open reduction internal fixation using a locked plating system versus plating and strut allograft with cerclage wiring to determine which treatment results in a faster return to function as measured by the TUG test at 6 weeks post-op.
Status | Recruiting |
Enrollment | 89 |
Est. completion date | June 2023 |
Est. primary completion date | June 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 90 Years |
Eligibility | Inclusion Criteria: - Age: over 18, no upper limit - Vancouver type B1 periprosthetic fracture - Fracture is amenable to either treatment group - Prosthesis is well fixed - Provision of informed consent Exclusion Criteria: - Presence of an active infection around the fracture (soft tissue or bone) - Loose prosthesis - Trauma patients with an ISS > 16 or associated major injuries of the lower extremities - Known substance abuse - Likely problems, in the judgment of the investigators, with maintaining follow-up (i.e., patients with no fixed address, report a plan to move out of town, or intellectually challenged patients without adequate family support) |
Country | Name | City | State |
---|---|---|---|
Canada | St. michael's Hospital | Toronto | Ontario |
Lead Sponsor | Collaborator |
---|---|
Unity Health Toronto |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | TUG test score at 6 weeks post-op | We will administer the TUG test to each patient at 6 weeks to determine if there is a difference in functional status between both groups. | 6 weeks | |
Secondary | Re-operation rates | We will measure rates of re-operationin each of the treatment groups on study specific case report forms. | 1 year |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02267330 -
Gonadal Radiation Exposure and Risk Secondary to Fluoroscopic Imaging During Trauma Surgery
|
||
Completed |
NCT03635320 -
The CHINA TFNA Study
|
N/A |