ASR™-XL Modular Acetabular Cup System
DeviceThe ASR™-XL Modular Acetabular Cup System treatment device is comprised of a metal acetabular cup, a unipolar femoral head and a taper sleeve adapter.
Other names: Acetabular cup replacement
NCT Number: NCT00561600
The primary objective of this investigation is to evaluate the clinical and radiographic outcomes of the ASR™-XL Acetabular Cup System compared to the Pinnacle™ Acetabular Cup with a 28mm or 36mm ULTAMET™ metal insert.
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Notify Me20 year–75 year
All sexes
Interventional
Not applicable
Desert Orthopaedics, Rancho Mirage, California, United States
The purpose of this clinical investigation is to gather sufficient clinical and radiographic data to permit valid scientific comparisons between treatment and control group outcomes. The treatment group/device for this study is the ASR™-XL Acetabular Cup System, and the control group/device is the Pinnacle™ Cup System w/ the 28mm or 36mm ULTAMET™ metal liner. The study objective will be achieved by way of treatment group selection, treatment administration, and management of participating study Subjects.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The ASR™-XL Modular Acetabular Cup System treatment device is comprised of a metal acetabular cup, a unipolar femoral head and a taper sleeve adapter.
Other names: Acetabular cup replacement
The Pinnacle™ shells are cementless, titanium alloy cups with Porocoat® porous coating and HA DuoFix™ coating. There are various different liners available for use with the Pinnacle™ Acetabular Cup System. For the purpose of this investigation, the CoCrMo ULTAMET® 28mm or 36 mm metal liners will be used.
Other names: Acetabular cup replacement
Time frame: 24-month interval.
"Composite success: 1) Revision free (life of study) 2) No evidence of radiographic failure (life of study) 3) Harris Hip score => 80 at 24 months"
Time frame: 24 months
T-Test of Harris Hip total score means at 24 months
Time frame: 24 months
Mean Harris Hip Pain sub score
Time frame: 24 months
Mean Harris Hip Function sub score at 24 months
Time frame: Pre-operative
Serum Cobalt
Time frame: pre-operative
Serum Chromium
Time frame: pre-operative
Erythrocyte cobalt
Time frame: Pre-operative
Erythrocyte Chromium
Time frame: 4 months post-operative
Serum Cobalt
Time frame: 4 months post operative
Serum Chromium
Time frame: 4 months post-operative
Erythrocyte Cobalt
Time frame: 4 months post-operative
Erythrocyte Chromium
Time frame: 12 months post-operative
Serum Cobalt
Time frame: 12 Months
Serum Chromium
Time frame: 12 Months
Erythrocyte Cobalt
Time frame: 12 months
Erythrocyte Chromium
Time frame: 24 months
Serum Cobalt
Time frame: 24 months
Serum Chromium
Time frame: 24 months
Erythrocyte Cobalt
Time frame: 24 months
Erythrocyte Chromium
Time frame: 36 months
Serum Cobalt
Time frame: 36 months
Serum Chromium
Time frame: 36 months
Erythrocyte cobalt
Time frame: 36 months
Erythrocyte chromium
Time frame: 48 months
Serum Cobalt
Time frame: 48 months
Serum Chromium
Time frame: 48 months
Erythrocyte Cobalt
Time frame: 48 months
Erythrocyte chromium
DePuy Orthopaedics
Industry
A Randomized, Prospective, Comparative, Multi-Center Clinical Evaluation of the DePuy ASR™-XL Acetabular Cup System vs. the Pinnacle™ Metal- on- Metal Total Hip System Study
Acronym: ASR
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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