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Anatomic Congruent Prosthetic Knee Design

NCT03633201 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 75

Last updated 2025-08-21

No results posted yet for this study

Summary

This double-blinded randomized control study will use kinematic and kinetic measures to compare an anatomical congruent prosthetic knee design to a standard prosthetic knee design. The patients will be measured pre- and post-operative and compared to a healthy non-osteoarthritis control group.

Conditions

Interventions

DEVICE

Cruciate Retaining

Zimmer Biomet's Personalized Knee system for knee osteoarthritis treatment. The standard insert.

DEVICE

Medial Congruent

Zimmer Biomet's Personalized Knee system for knee osteoarthritis treatment. The new anatomical congruent shaped insert.

Sponsors & Collaborators

  • Regional Hospital Holstebro

    collaborator OTHER

  • University of Aarhus

    lead OTHER

Principal Investigators

  • Maiken T Stilling, [email protected] · University clinic for hand, hip and knee surgery, Regional Hospital Holstebro, Aarhus University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-07-11
Primary Completion
2021-07-01
Completion
2026-09-01

Countries

  • Denmark

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 NCT03633201 on ClinicalTrials.gov