- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT03745976
Questionnaire and Radiography for Prosthesis Follow-up (Follow-up)
Evaluation of a New Long-term Total Articular Prosthesis Follow-up Strategy by Simple Questionnaire and Radiography
Ever-evolving prosthetic activity as described in a Swedish study that predicts 469 TKA per 10,000 inhabitants in 2130. Increased consultation of controls and post-arthroplasty follow-up is expected. There is a legal obligation to ensure long-term follow-up without official recommendation on follow-up procedures. The objective is to compare a consultation + Xray by the surgeon versus an Xray and a questionnaire completed by the patient who had a knee or hip replacement. This is to demonstrate the equivalence of both.
All patients who come back for an annual check of a prosthesis should complete this questionnaire and perform an X-ray of their prosthesis. The study lasts one year and includes all the patients with a previous knee or hip arthroplasty.
The result of the questionnaire and Xray will be compared to that of the consultation and Xray.
Visão geral do estudo
Status
Intervenção / Tratamento
Descrição detalhada
An english study published an article showing that a follow up by questionnaire versus a consultation was also effective.
For this study, investigator is going to take back all the patients having to return to consultation in 2017. . Normally at 3 months, 1, 3, 5, 10, 15 and 20 years post-operatively.
Thus investigator will be able to see the number of patients seen in consultation compared to the theoretical number The purpose of this study is to highlight the non-inferiority of the questionnaire compared to the consultation for screening for complications at 10 years.
If this proves to be the case, only complicating patients could be reviewed by calling them to the radio and their questionnaire.
Tipo de estudo
Inscrição (Real)
Contactos e Locais
Locais de estudo
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Clermont-Ferrand, França, 63003
- CHU Clermont-Ferrand
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Método de amostragem
População do estudo
Descrição
Inclusion Criteria:
- Patients who have had a primary total hip or total knee arthroplasty that must be seen again in 2017. Normally at 3 months, 1 years, 3, 5, 10, 15 and 20 years post-operatively
Exclusion Criteria:
- Patients who have previous complications with their joint replacement
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
Coortes e Intervenções
Grupo / Coorte |
Intervenção / Tratamento |
|---|---|
|
Group 1
a new long-term total articular prosthesis follow-up strategy by simple questionnaire and radiography (questionnaire and Xray for all patients)
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questionnaire and Xray for all patients
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Patients seen in consultation follow-up or not (yes / no).
Prazo: at 3 months
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Feasibility study of a new strategy of follow-up by questionnaire
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at 3 months
|
|
Patients seen in consultation follow-up or not (yes / no).
Prazo: at 1year
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Feasibility study of a new strategy of follow-up by questionnaire
|
at 1year
|
|
Patients seen in consultation follow-up or not (yes / no).
Prazo: at 3 years
|
Feasibility study of a new strategy of follow-up by questionnaire
|
at 3 years
|
|
Patients seen in consultation follow-up or not (yes / no).
Prazo: at 5 years
|
Feasibility study of a new strategy of follow-up by questionnaire
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at 5 years
|
|
Patients seen in consultation follow-up or not (yes / no).
Prazo: at 10 years
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Feasibility study of a new strategy of follow-up by questionnaire
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at 10 years
|
|
Patients seen in consultation follow-up or not (yes / no).
Prazo: at 15 years
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Feasibility study of a new strategy of follow-up by questionnaire
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at 15 years
|
|
Patients seen in consultation follow-up or not (yes / no).
Prazo: at 20 years
|
Feasibility study of a new strategy of follow-up by questionnaire
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at 20 years
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
economic impact (Number of working day)
Prazo: at 3 months, 1, 3, 5, 10, 15 and 20 years post-operatively.
|
Number of working day in days
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at 3 months, 1, 3, 5, 10, 15 and 20 years post-operatively.
|
|
economic impact (Number of consultations)
Prazo: at 3 months, 1, 3, 5, 10, 15 and 20 years post-operatively.
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Number of consultations with the surgeon,
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at 3 months, 1, 3, 5, 10, 15 and 20 years post-operatively.
|
|
economic impact (Number of radiography)
Prazo: at 3 months, 1, 3, 5, 10, 15 and 20 years post-operatively.
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Number of radiography realized by the patient
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at 3 months, 1, 3, 5, 10, 15 and 20 years post-operatively.
|
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economic impact (Cost phone call)
Prazo: at 3 months, 1, 3, 5, 10, 15 and 20 years post-operatively.
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According to the number of realized phone call
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at 3 months, 1, 3, 5, 10, 15 and 20 years post-operatively.
|
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Evaluation of the feasibility of the questionnaire for detection of certain complications
Prazo: at 3 months, 1, 3, 5, 10, 15 and 20 years post-operatively.
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Evaluation of the feasibility of the questionnaire method
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at 3 months, 1, 3, 5, 10, 15 and 20 years post-operatively.
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Roger ERIVAN, University Hospital, Clermont-Ferrand
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Real)
Conclusão do estudo (Real)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Outros números de identificação do estudo
- CHU-412
- 2018-A01022-53 (Outro identificador: 2018-A01022-53)
Informações sobre medicamentos e dispositivos, documentos de estudo
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