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Orthopedic Implant
ATTUNE Cementless PS Fixed Bearing for Knee Arthritis
N/A
Waitlist Available
Research Sponsored by DePuy Orthopaedics
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 5 years
Awards & highlights
No Placebo-Only Group
Summary
This trial will observe patients who have had the Attune Cementless Femur Tray (primary or revision procedures) to see if they meet the functional responder criteria.
Eligible Conditions
- Knee Arthritis
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~5 years
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Functional Responder Rate of first 225 Subjects
Secondary study objectives
EuroQol 5-Dimension 5-Level (EQ-5D-5L)
Forgotten Joint Score (FJS-12)
Frequency of Adverse Events
+9 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Active Control
Group I: ATTUNE Cementless PS Fixed BearingActive Control1 Intervention
Subjects enrolled who undergo TKA with the ATTUNE Cementless Fixed Bearing Posterior Stabilizing Configuration.
Group II: ATTUNE Cementless CR Fixed BearingActive Control1 Intervention
Subjects enrolled who undergo TKA with the ATTUNE Cementless Fixed Bearing Cruciate Retaining Configuration.
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Who is running the clinical trial?
DePuy OrthopaedicsLead Sponsor
80 Previous Clinical Trials
25,923 Total Patients Enrolled
Paul VoorhorstStudy DirectorDePuy Synthes
Allyson MorrisStudy DirectorDePuy Synthes
1 Previous Clinical Trials
1,542 Total Patients Enrolled
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