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Clinical Trial Summary

The purpose of this study was to compare the clinical (range of motion, weight bearing, quality of life) and radiographic outcome (boney consolidation) between open reduction and internal fixation using locking compression plates with revision prosthesis using a non-cemented long femoral stem in a group of patients with a Vancouver type-B2, B3 and C periprosthetic fracture after primary total hip replacement.


Clinical Trial Description

n/a


Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms


NCT number NCT02391129
Study type Observational
Source Medical University of Vienna
Contact
Status Completed
Phase N/A
Start date January 2014
Completion date January 2015

See also
  Status Clinical Trial Phase
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Recruiting NCT01973712 - Periprosthetic Distal Femur Fracture N/A
Not yet recruiting NCT03358186 - Investigation on the Surgical Treatment Effect of Periprosthetic Femur Fracture After Hip Arthroplasty N/A
Recruiting NCT06028971 - Safety and Performance of the Biphasic Plate Distal Femur: A Multicenter Case Series
Recruiting NCT04663893 - Peri-Implant and Peri-Prosthetic Fractures: Epidemiology, Morbidity, Mortality, Treatment and Outcome Analysis
Recruiting NCT03312088 - Maxx Orthopedics' PCK Revision TKA Study of Component Survivorship
Recruiting NCT03378557 - Periprosthetic Fracture Registry (PPFx)