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Biomet Humeral Stem Data Collection

NCT00553527 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2

Last updated 2009-08-06

No results posted yet for this study

Summary

The purpose of this prospective clinical data collection is to document the performance and clinical outcomes of Biomet Humeral Stems.

Conditions

  • Humeral Stem Replacement

Interventions

PROCEDURE

Humeral Stem replacement surgery

Patient will receive humeral stem replacement.

Sponsors & Collaborators

  • Vanderbilt University

    lead OTHER

Principal Investigators

  • Donald H Lee, MD · Vanderbilt University Medical Center

Study Design

Allocation
NON_RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-07-31
Primary Completion
2009-07-31
Completion
2009-07-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00553527 on ClinicalTrials.gov