Informations générales (source: ClinicalTrials.gov)

NCT02805803 En recrutement IDF
Quality of Life Assessment in Patients Undergoing Prolonged Suppressive Antibiotherapy for Prosthetic Joint Infection.
Interventional
  • Arthrite infectieuse
  • Maladies transmissibles
  • Infection
N/A
Groupe Hospitalier Diaconesses Croix Saint-Simon (Voir sur ClinicalTrials)
novembre 2016
juin 2025
17 septembre 2025
Prosthetic joint infection (PJI) management is complex and requires prosthesis replacement when symptoms duration is greater than 30 days or debridement with modular set replacement when symptoms duration is lesser than one month. Nevertheless, the prolonged suppressive antibiotherapy (PSA) is the single treatment we can provide to high risk surgical patients and those who refuse reoperation. There is limited data available on PSA modality, its tolerance and efficacy, this lack of data motivated us to concept a prospective study of long term patient follow up with PJI treated with prolonged suppressive antibiotherapy.
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Etablissements

Les établissements d'Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
GRPE HOSP DIACONESSES-CROIX ST-SIMON Simon MARMOR, MD En recrutement IDF Contact (sur clinicalTrials)
HOPITAL DE LA CROIX SAINT SIMON Younes KERROUMI, Doctorate En recrutement IDF Contact (sur clinicalTrials)

Critères

Tous
Inclusion Criteria:

- Patient aged over 18 years old with hip or knee prosthetic infection who consented
to participate in the study

- Non-eligible patient to surgical treatment

- Patient eligible to prolonged suppressive antibiotherapy



- patient who does not meet eligibility criteria

- Patient living or traveling abroad for whom 2 years minimum follow up is impossible.

- Patient lawfully deprived of his liberty

- Patient not insured under social security scheme