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

Not Applicable

Withdrawn

• Conditions: Rheumatoid Arthritis; Osteoarthritis; Traumatic Arthritis; Arthritis
• Interventions: Device: M2a-Magnum™ Large Metal Articulation; Device: Hip Resurfacing System

• Registration Number: NCT00585988
• Lead Sponsor: Biomet Orthopedics, LLC

Brief 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.

Detailed Description

Not available

Study Timeline

• Study Start: 2007-06
• Study First Submitted: 2007-12-21
• Study First Submitted QC: 2007-12-21
• Study First Posted: 2008-01-04
• Primary Completion: 2009-09
• Study Completion: 2010-09
• Status Verified: 2017-06
• Last Update Submitted: 2017-06-19
• Last Update Posted: 2017-06-21

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• Patients requiring hip arthroplasty

Exclusion Criteria

• Patients with sensory, neurological, or general health conditions that alter perception of their limb in space
• Patients with vestibular disorders

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
2	M2a-Magnum™ Large Metal Articulation	-
1	Hip Resurfacing System	-

Primary Outcome Measures

Name	Time	Method
Functional Tests	1 year