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Recruiting NCT04960098

Patient-reported Outcome Measures in Patient Underwent Total Hip and Knee Arthroplasty

— Observational Hip Osteoarthritis Knee Osteoarthritis Prosthesis Survival

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: arthroplasty.
Who it may be relevant to
Registry conditions: Hip Osteoarthritis, Knee Osteoarthritis, Prosthesis Survival. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Patient-Reported Outcome Measures in Patient Underwent Total Hip and Knee Arthroplasty in Galeazzi Orthopaedic Institute Milano

Overview

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.

Interventions

  • Procedure arthroplasty
    patient with hip and knee osteoarthritis underwent hip and knee arthroplasty

Primary outcome measures

  • outcome measurements [Time frame: pre operative to 10 years]

Eligibility criteria

Inclusion criteria

  • male and female
  • age more than 18
  • patient underwent hip or knee arthroplasty

Exclusion criteria

  • age less than 18
  • comorbidity that can results in the difficulty to come back for the follow up

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Italy · 1 center
  • Istituto Ortopedico Galeazzi — Milan

Identifiers

NCT: NCT04960098 · PROMS

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗