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

Zimmer Biomet

Status: Withdrawn

Conditions: Traumatic Arthritis; Osteoarthritis; Arthritis; Rheumatoid Arthritis

Treatments: Device: Hip Resurfacing System; Device: M2a-Magnum™ Large Metal Articulation

Study type: Interventional

Funder types: Industry

Identifiers

NCT00585988

292-U-010

Details and patient eligibility

About

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.

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

---

0 participants in 2 patient groups

1

Other group

Treatment:

Device: Hip Resurfacing System

2

Other group

Treatment:

Device: M2a-Magnum™ Large Metal Articulation