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Staphylococcal Acute Post-Operative PJI Treated With 'DAIR' And Impact Of Rifampin

Staphylococcal Acute Post-Operative Prosthetic Joint Infection Treated With 'DAIR' (Debridement and Implant Retention) And Impact Of Rifampin: A Retrospective Cohort Study In France

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03750721
Acronym
IPASTAPH
Enrollment
79
Registered
2018-11-23
Start date
2018-04-01
Completion date
2018-05-01
Last updated
2018-11-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Antibiotic Resistant Staphylococcus Aureus Infection, Bone and Joint Infection

Brief summary

S. aureus and coagulase-negative staphylococci are the most frequent bacteria responsible for PJI (prosthetic joint infection). The aim of this study is to describe the use of rifampicin.

Interventions

OTHERRole of rifampin in staphylococcal PJI

the aim is to determine if the dose and the duration of rifampin influenced the prognosis

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years

Inclusion criteria

patients having had acute PJI (i.e. \<1 month following the implantation), DAIR with exchange of removal components) due to S. aureus and coagulase-negative staphylococci (2011-2016)

Exclusion criteria

None

Design outcomes

Primary

MeasureTime frameDescription
description of the use of rifampicin : rate of useOutcome is measured at the end of follow-up (usually between 12 and 24 months after antibiotic therapy disruption)the aim is to determine how the use of rifampin influence the prognosis in staphylococcal acute post-operative prosthetic joint infection treated with DAIR

Secondary

MeasureTime frameDescription
rate of failure for treatment using rifampinOutcome is measured at the end of follow-up (usually between 12 and 24 months after antibiotic therapy disruption)Treatment failure is defined by local clinical and/or microbiological relapse; and/or need for additional surgery; death of septic origin
rate of adverse event with rifampinOutcome is measured at the end of follow-up (usually between 12 and 24 months after antibiotic therapy disruption)Description of adverses events leading to stop the rifampicin

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026