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Gender Solutions Natural Knee Post-Market Study

NCT01463566 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2019-01-09

No results posted yet for this study

Summary

This is a prospective multicenter study of the Gender Solutions Natural Knee Flex System when used in primary total knee arthroplasty. The purpose of the study is to obtain short-, Mid-, and long-term clinical outcomes and implant survivorship data for the Gender Solutions Natural Knee Flex System.

Conditions

Interventions

DEVICE

Zimmer Gender(R) Solutions(TM) Natural-Knee(R) Flex System

Gender Solutions Natural Knee Flex System in total knee arthroplasty

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Kacy Arnold, RN, MBA · Zimmer Biomet

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-01-31
Primary Completion
2024-07-31
Completion
2025-01-31

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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 NCT01463566 on ClinicalTrials.gov