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A Prospective Radiostereometric Analysis and Clinical Evaluation of the Zimmer® Continuum® Acetabular Cup With Vitamin E Stabilized Polyethylene
N/A
Waitlist Available
Led By Scott Sporer, MD
Research Sponsored by Central DuPage Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group
Summary
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.
Eligible Conditions
- Radiostereometric Analysis
- Zimmer Continuum Acetabular Cup
- Vitamin E Deficiency
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Vitamin E Polyethylene and RSAExperimental Treatment1 Intervention
All subjects will have the Vitamin E polyethylene and RSA beads placed during surgery. Subjects will then have standard x-ray images and RSA images taken at specific time points up until 2 years post-operatively.
Find a Location
Who is running the clinical trial?
Central DuPage HospitalLead Sponsor
14 Previous Clinical Trials
3,890 Total Patients Enrolled
Zimmer BiometIndustry Sponsor
378 Previous Clinical Trials
68,028 Total Patients Enrolled
Halifax Biomedical Inc.Industry Sponsor
1 Previous Clinical Trials
30 Total Patients Enrolled
Scott Sporer, MDPrincipal InvestigatorCentral DuPage Hospital
6 Previous Clinical Trials
340 Total Patients Enrolled