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Persona MC vs Attune Total Knee Replacement Study

NCT03580772 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 31

Last updated 2023-09-11

No results posted yet for this study

Summary

This study aims to compare clinical and functional outcomes of a cohort of patients that have undergone a medial congruent TKR to a similar cohort of patients that have undergone a conventional TKR and a cohort of control participants. Our null hypothesis is that there will be no difference in the functional outcome (as assessed by gait analysis) between Attune and Persona MC TKR.

Conditions

Interventions

DEVICE

Persona TKR

Persona® TKR (Zimmer Biomet)

DEVICE

Attune TKR

Attune® TKR (Depuy synthes)

Sponsors & Collaborators

  • Zimmer Biomet

    collaborator INDUSTRY

  • University of Leeds

    lead OTHER

Principal Investigators

  • Hemant Pandit, MBBS, MS · University of Leeds

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-11-26
Primary Completion
2019-12-04
Completion
2022-05-04
FDA Device
Yes

Countries

  • United Kingdom

Study Locations

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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 NCT03580772 on ClinicalTrials.gov