Comparison of Two Empirical Antimicrobial Therapies of Prosthetic Joint Infection

NCT ID: NCT03850860

Last Updated: 2023-09-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

178 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-12-01

Study Completion Date

2019-06-01

Brief Summary

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The empirical use of vancomycin in combination with a broad-spectrum beta-lactam is currently recommended after the initial surgery of prosthetic joint infection (PJI). However, the tolerability of such high-dose intravenous regimens is poorly known. T

Detailed Description

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The empirical use of vancomycin in combination with a broad-spectrum beta-lactam is currently recommended after the initial surgery of prosthetic joint infection (PJI). However, the tolerability of such high-dose intravenous regimens is poorly known. The empirical antimicrobial therapy of PJI is associated with an important rate of adverse, linked with the use of the vancomycin and the piperacillin-tazobactam combination. Some studies suggest to use vancomycin-cefepime, which remains to be evaluated in PJI.

Conditions

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Bone and Joint Infection

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

RETROSPECTIVE

Study Groups

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empirical antibotherapy currently used

patients having had a vancomycin and piperacillin-tazobactam combination as empirical antibiotherapy

empirical antibiotherapy

Intervention Type OTHER

comparison of the outcome in the 2 groups having had 2 different empirical antibiotherapies

another empirical antibotherapy

patients having had a vancomycin and cefepime combination as empirical antibiotherapy

empirical antibiotherapy

Intervention Type OTHER

comparison of the outcome in the 2 groups having had 2 different empirical antibiotherapies

Interventions

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empirical antibiotherapy

comparison of the outcome in the 2 groups having had 2 different empirical antibiotherapies

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* patients having had a prosthetic joint infection and having had a postoperative empirical antibiotherapy with combination of vancomycine and piperacillin-tazobactam or vancomycine and cefepime

Exclusion Criteria

* none
Minimum Eligible Age

18 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hospices Civils de Lyon

OTHER

Sponsor Role lead

Responsible Party

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Eugénie MABRUT

clinical research assistant

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Florent Valour, Md,PhD

Role: STUDY_DIRECTOR

HCL

Locations

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Hospices Civils de Lyon

Lyon, , France

Site Status

Countries

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France

Other Identifiers

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18-326

Identifier Type: -

Identifier Source: org_study_id

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