MedTrace Logo

Persona Partial Knee Clinical Outcomes Study

NCT03034811 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 757

Last updated 2026-04-22

No results posted yet for this study

Summary

The primary objective of this study is to obtain implant survivorship and clinical outcomes data for the commercially available Persona Partial Knee System.

Conditions

  • Osteoarthritis
  • Avascular Necrosis
  • Traumatic Arthritis
  • Conditional Tibial Condyle or Plateau Fractures
  • Conditional Revision of the Articular Surface

Interventions

DEVICE

Persona Partial Knee system

Fixed bearing partial knee

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Hillary Overholser · Zimmer Biomet

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-02-08
Primary Completion
2030-09-30
Completion
2030-09-30
FDA Device
Yes

Countries

  • United States
  • Austria
  • Belgium
  • France
  • Germany
  • Italy
  • Spain
  • Sweden
  • Switzerland
  • United Kingdom

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03034811 on ClinicalTrials.gov