Actively Recruiting
Mymobility Knee ROM
Led by Zimmer Biomet · Updated on 2026-01-20
41
Participants Needed
1
Research Sites
31 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This prospective study aims to evaluate the agreement, also referred as concordance, of the mymobilty knee ROM with a clinician's assessment of knee ROM via goniometer.
CONDITIONS
Official Title
Mymobility Knee ROM
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient is a minimum of 18 years of age
- Patient is willing and able to provide written Informed Consent by signing and dating the IRB-approved Informed Consent form
You will not qualify if you...
- The patient is currently participating in any other study that would hinder the assessor's ability to measure knee ROM
- Complex primary knee pathology with significant restrictions on the range of motion per surgeon discretion
- Patient is pregnant or considered a member of a protected population (e.g. prisoner, mentally incompetent, etc.)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Center for Advanced Orthopedics and Sports Medicine
Auburn Hills, Michigan, United States, 48326
Actively Recruiting
Research Team
E
Erik Kowalski, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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