Locking Compression Plate Fixation Versus Revision- Prosthesis of Vancouver-B2, B3 and C Periprosthetic Femoral Fractures After Total Hip Replacement

NCT ID: NCT02391129

Last Updated: 2015-03-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

102 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-01-31

Study Completion Date

2015-01-31

Brief Summary

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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.

Detailed Description

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Conditions

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Periprosthetic Fractures

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Hyperion Prosthesis

Patients treated with the second generation long-stem revision prosthesis

Operation for Periprosthetic fractures of the hip with stem loosening

Intervention Type PROCEDURE

Helios Prosthesis

Patients treated with the first generation long-stem revision prosthesis

Operation for Periprosthetic fractures of the hip with stem loosening

Intervention Type PROCEDURE

Locking compression plate

Patients treated with LCP

Operation for Periprosthetic fractures of the hip with stem loosening

Intervention Type PROCEDURE

Interventions

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Operation for Periprosthetic fractures of the hip with stem loosening

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patients with Vancouver type- BlI, BIII and C fractures and unstable femoral prosthesis stem.

Exclusion Criteria

* Patients with pathological fractures,
* Vancouver type-A, Bl, and
* stable femoral prosthesis stem,
* Patients with hemi - prosthesis and periprosthetic femoral fractures were excluded from final analysis.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Medical University of Vienna

OTHER

Sponsor Role lead

Responsible Party

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Julian Joestl

MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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1674/2014

Identifier Type: -

Identifier Source: org_study_id

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