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Evaluation of the Use of Cefoxitin in Combination in Continuous Parenteral Administration in the Treatment of Bone and Joint Infections

Evaluation of the Use of Cefoxitin in Combination in Continuous Parenteral Administration in the Treatment of Bone and Joint Infections

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03848104
Enrollment
35
Registered
2019-02-20
Start date
2018-01-01
Completion date
2018-04-01
Last updated
2019-02-22

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

Conditions

Antibiotic Reaction, Bone and Joint Infection

Keywords

cefoxitin, Bone and Joint Infection

Brief summary

Cephamycin related to 2nd generation cephalosporins, the use of cefoxitin has long been limited to antibiotic prophylaxis. Because of its spectrum (sensitive staphylococci, enterobacteria including ESBL, streptococci, anaerobes), its stability and its low cost, it could be useful in curative bone and joint infections, especially in case of infection polymicrobial disease in patients for whom antibiotic alternative per os is limited.

Interventions

OTHERbone and joint infection treated with cefoxitin

the patients had cefoxitin in combination in continuous parenteral administration to treat their bone / joint infection

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 havind had a bon and joint infeciton treated with cefoxitin in combination in continuous parenteral administration

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Rate of Treatment FailureOutcome is measured at the end of follow-up (usually between 12 and 24 months after antibiotic therapy disruptionTreatment failure is defined by local clinical and/or microbiological relapse; and/or need for additional surgery; death of septic origin

Secondary

MeasureTime frameDescription
Rate of use of this strategyOutcome is measured at the end of follow-up (usually between 12 and 24 months after antibiotic therapy disruptionDescriptions of patients managed with this strategy

Countries

France

Outcome results

None listed

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