Skip to content
Trial Eligibility
Menu

Z1 Hip System: Post-Market Clinical Follow Up Study

NCT07104279

This study is recruiting at 5 US sites in 5 states, according to its ClinicalTrials.gov record last updated .

Summary

The objectives of this study are to confirm the early to mid- term safety, performance, and clinical benefits of the Z1 Femoral Hip System in hemi- and primary total hip arthroplasty. Cohort 0 The primary endpoint is defined by the survival of the implant system at 2 years, which is based on the absence of removal of the study device and will be evaluated using a one-sample proportion as well as using the Kaplan Meier method.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Hip Osteoarthritis
  • Acute Traumatic Fracture of the Femoral Head or Neck
  • Avascular Necrosis of the Femoral Head

Eligibility basics and study details

Study type
Observational
Phase
Not applicable
Ages
18 years and older
Sex
All
Healthy volunteers
Not accepted
Sponsor
Zimmer Biomet
Last updated on ClinicalTrials.gov
October 16, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Missouri · 1

  • Mokan Orthopedic Research and Consulting · Platte City, MO

North Carolina · 1

  • OrthoCarolina/OrthoCarolina Research Institute · Charlotte, NC

Ohio · 1

  • Cleveland Clinic · Cleveland, OH

Oregon · 1

  • Orthopedic & Fracture Specialists · Portland, OR

Virginia · 1

  • Anderson Orthopaedic/Anderson Orthopaedic Research Institute · Alexandria, VA

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.