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Knee Hinge Prosthesis Following TKA Infection

Conditions
TKA Infection
Registration Number
NCT02856971
Lead Sponsor
Hospices Civils de Lyon
Brief Summary

Between 2009 and January 2016, the investigators included 49 patients from four hospitals in Lyon who had a Total Knee Arthroplasty (TKA) infection and who benefited of a knee arthroplasty revision with a rotating hinge prosthesis. This retrospective and descriptive cohort aims at studying the functional results after 2 years follow up.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
49
Inclusion Criteria
  • All the patients who had a rotating hinge knee arthroplasty for septic revision after total knee arthroplasty, proved by bacteriological samples or purulent drainage at involved site or other obvious clinical signs or radiological signs of infection
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Exclusion Criteria
  • Patients who benefited of a hinge prosthesis following a unicompartmental prosthesis, following a mechanical issue on a total prosthesis
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
functional resultsat two years follow up

Subjective functional results : satisfaction, patient expectations, functional activities. These items are based on the new IKS score

Secondary Outcome Measures
NameTimeMethod
infection controlafter 2 years follow up

presence or absence of clinical and/or biological signs of infection, recurrence of the infection or new secondary infection

Trial Locations

Locations (1)

Centre de reference des infections ostéo-articulaires de Lyon,Groupement Hospitalier Nord - Hôpital de la Croix-Rousse - Bât. B, niveau 3 103 Grande-Rue de la Croix-Rousse

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Lyon cedex 04, France

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