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Investigational Testing of Bodycad Unicompartmental Knee Prosthesis (UKS)

NCT03432481 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 28

Last updated 2023-08-25

No results posted yet for this study

Summary

This study is designed to observe clinical outcomes of patient-specific knee arthroplasty in patients with osteoarthritis of the medial condyle.

Conditions

  • Osteoarthritis, Knee

Interventions

PROCEDURE

Unicompartmental Knee Arthroplasty Surgery

Unicompartmental Knee Arthroplasty Surgery using the Bodycad Unicompartmental Knee System (BUKS)

DEVICE

Bodycad Unicompartmental Knee System (BUKS)

Unicompartmental Knee Arthroplasty Surgery using the Bodycad Unicompartmental Knee System (BUKS)

Sponsors & Collaborators

  • Laboratoires Bodycad Inc.

    lead INDUSTRY

Principal Investigators

  • Etienne Belzile, MD · CHU de Quebec - Hopital de l'Enfant-Jésus

  • Brian Hamlin, MD · Renaissance Orthopedics

  • Geoffroy Rivet-Sabourin, PhD · Laboratoires Bodycad Inc.

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
45 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-24
Primary Completion
2020-08-20
Completion
2023-03-07

Countries

  • Canada

Study Locations

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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 NCT03432481 on ClinicalTrials.gov