← Eichor
Study identifier: NCT04028687 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

MDR - PMCF Study for Taperloc Complete Stems

Condition: Hip Arthritis · Hip Disease · Hip Fractures  ·  Sponsor: Zimmer Biomet

PhaseN/A
Planned participants820
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The objective of this consecutive series PMCF study is to collect data confirming safety, performance, and clinical benefits of the Taperloc Complete stems when used for primary or revision total hip arthroplasty (implants) at 1,3,5,7 and 10-year follow-up\*. Since Taperloc Complete was introduced to the EU in 2010, all available retrospective data will be collected from each patient and a prospective aspect to the study will be necessary to reach the 10-year time point.

This description comes directly from the study's public registry record.

Talk to the study team

Megan McKinnie  ·  +1 (919) 381-7091  ·  megan.mckinnie@zimmerbiomet.com

Lynsey Boyle  ·  +1 (412) 552-7111  ·  Lynsey.Boyle@zimmerbiomet.com

Always discuss trial participation with your own doctor first.

Locations (3)

Orthopaedic Institute of HendersonHenderson, Nevada, United StatesWithdrawn
Texas Health Physicians GroupPlano, Texas, United StatesRecruiting
Proliance Orthopaedics and Sports MedicineBellevue, Washington, United StatesWithdrawn

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT04028687