Mymobility Knee ROM
ConditionKnee Range of Motion
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorZimmer Biomet
About this trial
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.
Eligibility criteria
Qualifiers
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
Disqualifiers
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.)
Trial design
Treatments tested in this trial
- Not listed
Trial groups
41 Participants
are grouped into 1 trial groupSponsors and collaborators
Source ClinicalTrials.gov