Types of Fixation of Vancouver B1 Periprosthetic Fractures

Sponsor
Unity Health Toronto (Other)
Overall Status
Recruiting
CT.gov ID
NCT01354535
Collaborator
(none)
89
1
2
123.9
0.7

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Isolated Locked Compression Plate
  • Procedure: Cable Plating and Strut Allograft with Cerclage Wiring
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
89 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
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
Study Start Date :
Feb 1, 2013
Anticipated Primary Completion Date :
Jun 1, 2023
Anticipated Study Completion Date :
Jun 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Cable plating with strut

The plate will be placed laterally with the allograft strut placed on the anterior cortex. Screw fixation will be used distal to the stem and cables and screws will be used proximal to the stem tip. Cerclage cables or wires will be used to secure the strut.

Procedure: Cable Plating and Strut Allograft with Cerclage Wiring
The plate will be placed laterally with the allograft strut placed on the anterior cortex. Screw fixation will be used distal to the stem and cables and screws will be used proximal to the stem tip. Cerclage cables or wires will be used to secure the strut.

Active Comparator: isolated plating

A lateral thigh incision will be used to expose the fracture site. Surgeons will attempt to minimize devascularization of the bone by meticulous dissection and indirect reduction techniques. An appropriate sized plate will be applied to the lateral aspect of the femur. Fracture reduction will be achieved with the use of intra-operative fluoroscopy and the plate will be secured with locking screws.

Procedure: Isolated Locked Compression Plate
A lateral thigh incision will be used to expose the fracture site. Surgeons will attempt to minimize devascularization of the bone by meticulous dissection and indirect reduction techniques. An appropriate sized plate will be applied to the lateral aspect of the femur. Fracture reduction will be achieved with the use of intra-operative fluoroscopy and the plate will be secured with locking screws.

Outcome Measures

Primary Outcome Measures

  1. TUG test score at 6 weeks post-op [6 weeks]

    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.

Secondary Outcome Measures

  1. Re-operation rates [1 year]

    We will measure rates of re-operationin each of the treatment groups on study specific case report forms.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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)

Contacts and Locations

Locations

Site City State Country Postal Code
1 St. michael's Hospital Toronto Ontario Canada M5C 1R1

Sponsors and Collaborators

  • Unity Health Toronto

Investigators

  • Principal Investigator: Emil Schemitsch, MD, FRCS(C), Unity Health Toronto
  • Principal Investigator: Aaron Nauth, MD, FRCSC, Unity Health Toronto

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Unity Health Toronto
ClinicalTrials.gov Identifier:
NCT01354535
Other Study ID Numbers:
  • 13052011
First Posted:
May 17, 2011
Last Update Posted:
Jun 18, 2021
Last Verified:
Jun 1, 2021
Keywords provided by Unity Health Toronto
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 18, 2021