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OpenTrials
Completed

NCT Number: NCT00873145

Management of Bone Defects Around the Elbow

Background:

Bone defects of the distal humerus require complex reconstructions, for which standard prostheses may be insufficient. The researchers therefore investigated the clinical and radiological outcome of elbow reconstructions by megaprostheses.

Completed

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Medical University of Vienna Department of Orthopaedics

Vienna, 1090, Austria

About this study

Type of prosthesis:

STRYKER Humerus-HMRS

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • HMRS of the elbow, distal humerus or total humerus

Exclusion criteria

  • Unwillingness to participate

Treatment and study plan

HMRS

Procedure

Modular prosthetic replacement of the humerus and elbow.

Primary outcomes

  1. Patient Survival

    Time frame: 20 Years

Secondary outcomes

  1. Prosthetic Survival

    Time frame: 20 Years

Sponsors and collaborators

Lead sponsor

Medical University of Vienna

Other

Registry information

Official study title

Modular Prosthetic Reconstruction of Major Bone Defects of the Distal Humerus.

Important dates

Study start
2008
Primary completion
2009
Study completion
2010
First posted
Apr 1, 2009
Registry last updated
Apr 15, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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