Fracture of Distal Femur Clinical Trial
Official title:
MotionLoc Study: Healing of Distal Femur Fractures Stabilized With a Flexible Plating Construct Using MotionLoc Screws
Verified date | January 2013 |
Source | Legacy Biomechanics Laboratory |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Legacy IRB |
Study type | Observational |
The objective of this study is to document callus formation and healing of fractures stabilized with locking plates utilizing modern MotionLoc screws that provide controlled axial micro-motion to actively promote fracture healing.
Status | Completed |
Enrollment | 33 |
Est. completion date | January 2013 |
Est. primary completion date | May 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 17 Years and older |
Eligibility |
Inclusion Criteria: 1. Patients with distal femur fracture (AO/OTA Type 33A and 33C) 2. Patients 17 years of age and over. 3. Patients able to be operated on by selected surgeons at the participating centers. Exclusion Criteria: 1. Pregnancy 2. Patients who are enrolled in an investigational treatment trial. 3. Patients who are not expected to survive the follow-up period. 4. Considered an inappropriate participant by the study physician. 5. Revision surgery 6. Patients currently incarcerated or awaiting incarceration. 7. Severe spinal injury with neurological deficit resulting in paralysis. 8. Fracture fixed more then 28 days after injury. 9. Acute or chronic local or systemic infections 10. Periprosthetic fractures |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
United States | Legacy Health System | Portland | Oregon |
Lead Sponsor | Collaborator |
---|---|
Legacy Biomechanics Laboratory | Slocum Center for Orthopaedics, Eugene, OR, University of Utah, Zimmer, Inc. |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Fracture Healing | Fracture healing is defined clinically by the ability of pain-free weight bearing, and radiographically by callus formation and bridging. | 6, 12, and 24 weeks post surgery | No |
Secondary | Periosteal Callus Size | Periosteal callus size is assessed at the anterior, posterior, and medial aspects on radiographs using a validated computational algorithm. | 6, 12, 24 weeks post surgery | No |
Secondary | Bridging Callus from CT | Cross-sectional image analysis, supported by 3-D rendering, to detect bony bridging at the anterior, posterior, and lateral aspects of the femur. | 12 weeks post surgery | No |
Secondary | Fixation Failure | Assessed in terms of loss of alignment at 12 and 24 weeks post surgery | 24 weeks post surgery | No |
Secondary | Hardware failure | Breakage of screw or plate | 6, 12, 24 weeks post surgery | No |