Retrospective Clinical and Functional Evaluation of Patients Undergoing Knee Replacement With Small Implants

Overview

Retrospective evaluation of: Functional results Clinical results Survivorship of knee replacement performed with small implants, isolated or combined

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: N/A
    • Intervention Model: Single Group Assignment
    • Primary Purpose: Treatment
    • Masking: None (Open Label)
  • Study Primary Completion Date: January 1, 2022

Detailed Description

Retrospective evaluation of partial knee replacements (medial UNI, lateral UNI, patellofemoral replacement, combined UNI+ patellofemoral replacement, combined medial and lateral UNI) performed in the Joint Replacement Department of the IRCCS Istituto Ortopedico Galeazzi. evaluation includes: clinical examination, functional results, survivorship at 1, 2, 5 , 10 and 15 years.

Interventions

  • Procedure: PARTIAL KNEE REPLACEMENT
    • PARTIAL KNEE REPLACEMENT

Arms, Groups and Cohorts

  • Experimental: partial knee replacement
    • medial UNI, lateral UNI, patellofemoral replacement, combined UNI+ patellofemoral replacement, combined medial and lateral UNI

Clinical Trial Outcome Measures

Primary Measures

  • KNEE SOCIETY SCORE
    • Time Frame: 2 years
    • total scale range: 0 (minimum)-100 (maximum); excellent results: 80-100
  • KNEE SOCIETY SCORE
    • Time Frame: 5 years
    • total scale range: 0 (minimum)-100 (maximum); excellent results: 80-100
  • KNEE SOCIETY SCORE
    • Time Frame: 10 years
    • total scale range: 0 (minimum)-100 (maximum); excellent results: 80-100

Participating in This Clinical Trial

Inclusion Criteria

  • patients receiving medial UNI or lateral UNI or patellofemoral replacement or combined UNI+ patellofemoral replacement or combined medial and lateral UNI – age > 18 years exclusion criteria – patients receiving total knee replacement – patients having revision or a knee replacement

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • I.R.C.C.S Ospedale Galeazzi-Sant’Ambrogio
  • Provider of Information About this Clinical Study
    • Sponsor

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