Informations générales (source: ClinicalTrials.gov)

NCT03611634 Statut inconnu
Consitution Of A Biological Collection From Samples From The Gut Microbiote In Patients Having A Bone Or Joint Infection Treated By A Suppressive Subcutaneous Antibiotherapy With Betalactamine
Observational
  • Arthrite infectieuse
  • Maladies transmissibles
  • Infection
Hospices Civils de Lyon (Voir sur ClinicalTrials)
juillet 2018
juillet 2024
27 juillet 2024
Optimal surgical therapy (debridement in chronic osteomyelitis; device exchange in patients with chronic prosthetic joint infection [PJI]) could be sometimes non-feasible, especially in the elderly population. Therefore, a medical therapy with oral prolonged suppressive antibiotic therapy (PSAT) seems to be an option to prevent recurrence and prosthesis loosening. Unfortunately, some patients are infected with resistant pathogens for which oral antibiotics are not suitable. Subcutaneous (SC) administration of injectable intravenous antibiotics as PSAT could be a convenient way to limit catheter-related complications and facilitate ambulatory care. However, there are few data concerning the development of resistance under subcutaneous prolonged treatment with betalactamine. The aim of this study is is just to constitute a biological collection from samples from the GUT microbiote in patients having a bone or joint infection treated by a suppressive subcutaneous antibiotherapy with betalactamine. Later analysis will be led on those samples to detect the acquisition of resistance or not.

Etablissements

Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
Hospices Civils de Lyon - 69004 - Lyon - France Eugenie Mabrut, CRA En recrutement Contact (sur clinicalTrials)

Critères

Tous
Inclusion Criteria:

- Patients having an ostéo-articular infection (on material or on native bone) and
having an indication of antibiotic treatment suppressive subcutaneous by
betalactamine and managed at the Croix-Rousse Hospital

- Patients not opposed to participate to the study



- none