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Far Cortical Locking Versus Standard Constructs for Distal Femur Fractures (FCL)

Primary Purpose

Distal Femur Fracture

Status
Active
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Far Cortical locking screw fixation
Standard screw fixation
Sponsored by
University of British Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Distal Femur Fracture focused on measuring Distal, Femur, Locking, Screw, Fracture, Healing

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Specific inclusion criteria:

  • Men or women ages 18 years or older
  • Displaced distal femur fracture (OTA 33A or 33C) as seen in radiographs
  • Planned treatment using a distal femur locking plate
  • Ability to read and speak English or availability of translator willing to assist with completion of study forms
  • Fractures < 14 days post injury
  • Provision of informed consent

Specific exclusion criteria:

  • Open distal femur fracture requiring flap or vascular repair (grade 3b or 3c)
  • Planned fixation strategy includes interfragmentary lag fixation of non-articular fractures
  • Active local infection
  • Limited life expectancy due to significant medical co-morbidity or medical contraindication to surgery
  • Inability to comply with rehabilitation or form completion
  • Likely problems, in the judgment of the investigators, with maintaining follow-up (i.e. patients with no fixed address, patients not mentally competent to give consent, etc.)
  • Non-ambulatory patients
  • Lack of bone substance or poor bone quality which, in the surgeon's judgment, makes locked plate fixation impossible
  • Periprosthetic fractures
  • Any concomitant lower-extremity injury that requires non-weight-bearing beyond 6 weeks post-operative
  • Addition of bone graft, bone graft substitute or BMP
  • Pregnant women

Sites / Locations

  • Vancouver General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Far Cortical Locking screw fixation

Standard screw fixation

Arm Description

Far Cortical Locking screw fixation

Standard screw fixation

Outcomes

Primary Outcome Measures

Composite fracture healing
Radiographic fracture healing defined as bridging of 1 or more cortices. Clinical fracture healing assessed with FIX-IT. Using the win ratio method, we hierarchically assessed radiographic healing, followed by clinical fracture healing. The pairwise comparison proceeds in a hierarchical fashion, using radiographic healing, followed by the FIX-IT score when patients cannot be differentiated based on radiographic healing. For each pairwise comparison, the treatment groups are assigned a win, loss, or tie. We calculate the win ratio as the number of wins in the FCL screw treatment group divided by the number of wins in the Standard screw group.

Secondary Outcome Measures

Radiographic healing
Union is defined as the bridging of 1 or more cortices with stable fixation by three months post-fixation.
Clinical healing
We assessed clinical fracture healing using the Function Index for Trauma (FIX-IT) score. The FIX-IT instrument quantifies clinical healing by aggregating a 0- to 6-point assessment of weight-bearing and fracture site pain for a maximum score of 12 points, indicating the highest level of functional healing.
Patient-reported health-related quality of life
Assessment of SF-36 scores (physical component and mental component)
Patient-reported health-related quality of life
Assessment of SF-36 scores (physical component and mental component)
CT quantification of fracture callus volume
Using a quantitative protocol, the volume of callus will be measured.

Full Information

First Posted
January 9, 2013
Last Updated
October 13, 2022
Sponsor
University of British Columbia
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1. Study Identification

Unique Protocol Identification Number
NCT01766648
Brief Title
Far Cortical Locking Versus Standard Constructs for Distal Femur Fractures
Acronym
FCL
Official Title
A Multicentre, Randomized Trial of Far Cortical Locking Versus Standard Constructs for Acute, Displaced Fractures of the Distal Femur Treated With Locked Plate Fixation
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 2013 (Actual)
Primary Completion Date
May 2022 (Actual)
Study Completion Date
April 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of British Columbia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To determine if Far Cortical Locking screws increase fracture healing rates at 3 months in Closed Distal Femur Fractures in adults when compared to Standard screw constructs. Fracture healing at 3 months will be assessed via radiographic and clinical assessment of the fracture. Null Hypothesis: There will be no difference in fracture healing at 3 months post-fixation between subjects treated with far cortical locking screw or standard screw fixation.
Detailed Description
A multicentre randomized controlled trial with a sample size of 138 subjects. Primary Outcome is fracture healing at 3 months via radiographic and and clinical assessment. Radiographic healing will be defined as bridging of one or more cortices as seen on x-ray. Radiographic assessment will be centrally adjudicated by a committee of three study investigators. Clinical healing will be assessed using the Function Index for Trauma (FIX-IT). Secondary outcome measurements will include patient-reported quality of life and CT quantification of fracture callus volume. Quality of life will be measured with the Short-Form 36 Version 2 (SF-36) instrument at all follow-up intervals. A CT scan of the fracture site will be performed at the 3 month follow-up. Using a quantitative protocol the volume of callus will be measured and the extent of cortical bridging will be assessed. Additional secondary outcomes include radiographic and clinical healing, as well as patient-important complications. These will include adverse events, delayed union (>6 months), non union (failure for fracture healing to progress on serial x-rays between 6 and 9 months), malalignment (>5 degrees), hardware failure, infection, and reoperation. Information surrounding the type of complication, duration, management and/or treatment of all complications will be recorded A Data Safety Monitoring Board will be established to independently monitor trial data. Specific inclusion criteria: Men or women ages 18 years or older Displaced distal femur fracture (OTA 33A or 33C) as seen in radiographs Planned treatment using a distal femur locking plate Ability to read and speak English or availability of translator willing to assist with completion of study forms Fractures < 14 days post injury Provision of informed consent Specific exclusion criteria: Open distal femur fracture requiring flap or vascular repair (grade 3b or 3c) Planned fixation strategy includes interfragmentary lag fixation of non-articular fractures Active local infection Limited life expectancy due to significant medical co-morbidity or medical contraindication to surgery Inability to comply with rehabilitation or form completion Likely problems, in the judgment of the investigators, with maintaining follow-up (i.e. patients with no fixed address, patients not mentally competent to give consent, etc.) Non-ambulatory patients Lack of bone substance or poor bone quality which, in the surgeon's judgment, makes locked plate fixation impossible Periprosthetic fractures Any concomitant lower-extremity injury that requires non-weight-bearing beyond 6 weeks post-operative Addition of bone graft, bone graft substitute or BMP Pregnant women

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Distal Femur Fracture
Keywords
Distal, Femur, Locking, Screw, Fracture, Healing

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
167 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Far Cortical Locking screw fixation
Arm Type
Experimental
Arm Description
Far Cortical Locking screw fixation
Arm Title
Standard screw fixation
Arm Type
Active Comparator
Arm Description
Standard screw fixation
Intervention Type
Device
Intervention Name(s)
Far Cortical locking screw fixation
Intervention Description
Standard screw fixation
Intervention Type
Device
Intervention Name(s)
Standard screw fixation
Primary Outcome Measure Information:
Title
Composite fracture healing
Description
Radiographic fracture healing defined as bridging of 1 or more cortices. Clinical fracture healing assessed with FIX-IT. Using the win ratio method, we hierarchically assessed radiographic healing, followed by clinical fracture healing. The pairwise comparison proceeds in a hierarchical fashion, using radiographic healing, followed by the FIX-IT score when patients cannot be differentiated based on radiographic healing. For each pairwise comparison, the treatment groups are assigned a win, loss, or tie. We calculate the win ratio as the number of wins in the FCL screw treatment group divided by the number of wins in the Standard screw group.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Radiographic healing
Description
Union is defined as the bridging of 1 or more cortices with stable fixation by three months post-fixation.
Time Frame
3 months
Title
Clinical healing
Description
We assessed clinical fracture healing using the Function Index for Trauma (FIX-IT) score. The FIX-IT instrument quantifies clinical healing by aggregating a 0- to 6-point assessment of weight-bearing and fracture site pain for a maximum score of 12 points, indicating the highest level of functional healing.
Time Frame
3 months
Title
Patient-reported health-related quality of life
Description
Assessment of SF-36 scores (physical component and mental component)
Time Frame
3 months
Title
Patient-reported health-related quality of life
Description
Assessment of SF-36 scores (physical component and mental component)
Time Frame
12 months
Title
CT quantification of fracture callus volume
Description
Using a quantitative protocol, the volume of callus will be measured.
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Specific inclusion criteria: Men or women ages 18 years or older Displaced distal femur fracture (OTA 33A or 33C) as seen in radiographs Planned treatment using a distal femur locking plate Ability to read and speak English or availability of translator willing to assist with completion of study forms Fractures < 14 days post injury Provision of informed consent Specific exclusion criteria: Open distal femur fracture requiring flap or vascular repair (grade 3b or 3c) Planned fixation strategy includes interfragmentary lag fixation of non-articular fractures Active local infection Limited life expectancy due to significant medical co-morbidity or medical contraindication to surgery Inability to comply with rehabilitation or form completion Likely problems, in the judgment of the investigators, with maintaining follow-up (i.e. patients with no fixed address, patients not mentally competent to give consent, etc.) Non-ambulatory patients Lack of bone substance or poor bone quality which, in the surgeon's judgment, makes locked plate fixation impossible Periprosthetic fractures Any concomitant lower-extremity injury that requires non-weight-bearing beyond 6 weeks post-operative Addition of bone graft, bone graft substitute or BMP Pregnant women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kelly Lefaivre, MD
Organizational Affiliation
University of British Columbia, Vancouver Coastal Health Authority
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vancouver General Hospital
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V5Z 1M9
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
36197809
Citation
Claireaux HA, Searle HK, Parsons NR, Griffin XL. Interventions for treating fractures of the distal femur in adults. Cochrane Database Syst Rev. 2022 Oct 5;10(10):CD010606. doi: 10.1002/14651858.CD010606.pub3.
Results Reference
derived

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Far Cortical Locking Versus Standard Constructs for Distal Femur Fractures

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