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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