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MDR - PMCF Study for Taperloc Complete Stems
Sponsor: Zimmer Biomet
Summary
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.
Official title: Post Market Clinical Follow up Study to Provide Safety, Performance and Clinical Benefits Data of the Taperloc Complete Stems
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
820
Start Date
2020-02-13
Completion Date
2032-02-12
Last Updated
2025-03-11
Healthy Volunteers
No
Interventions
Taperloc Complete Stem
Patients that have been implanted with a Taperloc Complete Stem to improve hip malfunction/disease.
Locations (3)
Orthopaedic Institute of Henderson
Henderson, Nevada, United States
Texas Health Physicians Group
Plano, Texas, United States
Proliance Orthopaedics and Sports Medicine
Bellevue, Washington, United States