Mymobility Knee ROM

Completed

Conditions studied: Knee Range of Motion

In brief

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.

Key facts

Study ID

NCT06863428

Run by

Zimmer Biomet

People needed

41

Starts

2025-11-21

Expected to finish

2026-03-09

Last updated by the study team

2026-07-10

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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 may not qualify if…

• 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.)

Where it is running

• Center for Advanced Orthopedics and Sports Medicine — Auburn Hills, Michigan, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.