Patient-reported Outcome Measures in Patient Underwent Total Hip and Knee Arthroplasty
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorI.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
About this trial
Registry of Galeazzi Orthopedic Institute: provides for the regular and systematic collection of all data (clinical and some PROMs) obtained from patients undergoing hip and knee arthroplasty to which questionnaires are proposed investigating the specific functional sphere of the joints undergoing surgery (Knee injuryOsteoarthritisOutcomeScore (KOOS-PS) and Hip injuryOsteoarthritisOutcomeScore (HOOS-PS) but also the sphere of general health (ShortForm health survey-12 (SF-12) and VisualAnalogueScale (VAS)) , in addition, of course, to the satisfaction rate.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
male and female
age more than 18
patient underwent hip or knee arthroplasty
Disqualifiers
age less than 18
comorbidity that can results in the difficulty to come back for the follow up
Trial population
All patients underwent hip and knee arthroplasty included in inclusion criteria
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
arthroplasty
Procedure/Surgerypatient with hip and knee osteoarthritis underwent hip and knee arthroplasty
Treatment groups
5,816 Participants
are divided into 1 treatment groupGroup A: patient underwent hip and knee arthroplasty1 intervention
Trial outcomes
Primary outcomes
1
outcome measurements
improve evaluation of hip and knee arthroplasty monitoring patient reported outcome measurements before and after surgery.
Time frame
pre operative to 10 yearsSponsors and contacts
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Source ClinicalTrials.gov