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Trident II Tritanium Acetabular Shell Outcomes Study

Terminated · Not applicable · NCT02999009

Conditions: Arthroplasty, Replacement, Hip

At a glance

Research payments reported, 2025
$19,083
U.S. investigators named
5
Sites paid
6
Planned or actual enrollment
383

About the trial

Sponsor
Stryker Orthopaedics
Tested
Trident II Tritanium Acetabular Shell (device)
Dates
Started 2017-01-20; completion 2026-08-24
Results posted
Not yet

The purpose of this study is to review the performance and success rate of an FDA approved cementless hip replacement part called the Trident II Tritanium Acetabular Shell. The study will specifically look at the need to revise the hip replacement after 5 years. This will be compared to how much this happens in patients who have hip replacement with similar cementless acetabular shells.

From ClinicalTrials.gov, last updated 2026-10-27. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Stryker Corporation reported $19,083 in research payments for this study in 2025 (22 payments).

Products named: Triathlon, Trident, Tritanium

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

  • Michigan Heart $7,235
  • American Orthopedic Foundation $5,560
  • $1,800
  • The Feinstein Institutes for Medical Research $1,697
  • Center for Orthopaedics and Spine LLC $1,336
  • Rothman Orthopaedics Rothman Institute $1,077
  • Hospital for Special Surgery, NY $377

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