Winfield, Illinois 60190

  • Zimmer® Continuum® Acetabular Cup

Purpose:

The purpose of this study is to use Radiostereometric Analysis (RSA) and clinical outcome measures to evaluate early, post-operative implant stability, post-operative implant fixation, clinical performance, and in-vivo wear of the Zimmer® Continuum® Cup with vitamin E stabilized polyethylene.


Criteria:

Inclusion Criteria: - Symptomatic osteoarthritis of the hip indicating surgical intervention - Scheduled to undergo an uncemented total hip arthroplasty (THA) - Patients between the ages of 18 and 65, inclusive - Ability to give informed consent - Patients will be available for follow-up for a minimum of 2 years after surgery Exclusion Criteria: - Patients less than 18 years of age, or older than 65 years of age. - Post-traumatic arthritis in the affected hip - Rheumatoid arthritis in the affected hip - Hip dysplasia in the affected hip - Prior arthroplasty of the affected hip - Active or prior infection of the affected hip - Morbid obesity (BMI > 35) - Medical condition precluding major surgery - Severe osteoporosis or osteopenia - Neuromuscular impairment - Patients with known allergy to metals - Pregnancy - Patients with compromised kidney function - Patient is immuno-suppressed - Patients that require a femoral head less than 32 mm or greater than 40mm.


NCT ID:

NCT01754155


Primary Contact:

Principal Investigator
Scott Sporer, MD
Central DuPage Hospital

Stefanie Miller
Phone: 630-933-6254
Email: Stefanie.Miller@CadenceHealth.org


Backup Contact:

Email: Judy.Guerreiro@CadenceHealth.org
Judy Guerreiro
Phone: 630-933-2941


Location Contact:

Winfield, Illinois 60190
United States

Miller
Phone: 630-933-6254

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: September 26, 2021

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