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
This trial accepts healthy volunteersQualifiers
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 population
The study population will consist of a minimum of 41 patients who meet all the inclusion criteria and none of the exclusion criteria.
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
41 Participants
are grouped into 1 trial groupGroup A: Group 1
Trial outcomes
Primary outcomes
1
Active knee flexion
Patients will be asked to sit in a chair to measure full active knee flexion.
Time frame
Day 1 (Single Visit)2
Active knee extension
Patients will be asked to sit in a chair to measure full active knee extension.
Time frame
Day 1 (Single Visit)3
Passive knee extension with overpressure
Patients will be asked to sit in a chair to measure full passive knee extension while applying overpressure on their knee with their hands.
Time frame
Day 1 (Single Visit)Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov