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Restoration® Anatomic Dual Mobility (ADM) X3® Acetabular System Study

Terminated · Not applicable · NCT01420237

Conditions: Arthroplasty, Replacement, Hip

At a glance

Research payments reported, 2025
$6,301
U.S. investigators named
4
Sites paid
4
Planned or actual enrollment
367

About the trial

Sponsor
Stryker Orthopaedics
Tested
Restoration ADM X3 Device (device)
Dates
Started 2011-06; completion 2023-11-09
Results posted
Yes

The purpose of this study is to evaluate the success rate of cementless primary hip replacement with the Restoration® ADM X3® Acetabular System as compared to other primary hip systems in the literature, through absence of femoral head dislocation at 10 years postoperative.

From ClinicalTrials.gov, last updated 2025-01-22. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Stryker Corporation reported $6,301 in research payments for this study in 2025 (4 payments).

Products named: Accolade, X3, Restoration

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.