A Study of Static versus Articulating Antibiotic Spacer for Periprosthetic Joint Infection in Total Knee Arthroplasty

Overview

Información sobre este estudio

What is the difference in the outcomes of patients treated with an articulating antibiotic spacer versus a static articulating spacer in the setting of two stage exchange for an infected total knee arthroplasty?

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria

  • Male or female
  • Age 18 to 100 years of age.
  • Preoperative diagnosis of bacterial infection by culture which would include a preoperative aspiration and at least three intraoperative cultures
    • The preoperative aspiration would also be sent for a cell count with differential
    • All patients would have an ESR and CRP drawn in the preoperative phase
    • Patients with a negative preoperative aspiration, but an actively draining wound or draining sinus tract, would be considered as infected
    • Intraoperative histopathology would also be obtained in all cases of infected total knee replacement at the time of the resection.
  • Intact extensor mechanism.
  • Adequate soft tissue envelope (no requirement for soft tissue coverage such as a muscle flap or skin graft)
  • Adequate bone stock for knee reconstruction
  • Medical fitness for staged knee reconstruction

 

Exclusion Criteria

  • Known atypical infection (mycobacterial or fungal)
  • Extensor mechanism disruption
  • Inadequate soft tissue envelope requiring muscle flap or skin grafting
  • Inadequate bone stock (T3 or F3 by the AORI classification)
  • Medical status precluding staged knee reconstruction
  • Requirement for hinged knee reconstruction at the time of reimplantation
  • Pregnant women
    • women of child bearing age will need a negative pregnancy test prior to enrollment to the study.

 

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus

Rochester, Minn.

Investigador principal de Mayo Clinic

Michael Taunton, M.D.

Cerrado para la inscripción

More information

Publicaciones

Publications are currently not available

Información adicional de contacto

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Teléfono: 800-664-4542 (llamada gratis)

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