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A Clinical Investigation of Recovery Following Hip Resurfacing or Total Hip Arthroplasty

NCT00585988 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2017-06-21

No results posted yet for this study

Summary

The primary purpose of this study is to compare early functional outcomes in patients undergoing hip resurfacing and total hip arthroplasty with the M2a-Magnum™ using more objective measures of function.

Conditions

Interventions

DEVICE

Hip Resurfacing System

This arm will utilize a hip resurfacing system.

DEVICE

M2a-Magnum™ Large Metal Articulation

This arm will utilize the M2a-Magnum™ implant system.

Sponsors & Collaborators

  • Biomet Orthopedics, LLC

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-06-30
Primary Completion
2009-09-30
Completion
2010-09-30

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Entities

Diseases

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 NCT00585988 on ClinicalTrials.gov