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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06113107
Other study ID # 8786
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 1, 2023
Est. completion date March 13, 2024

Study information

Verified date October 2023
Source University Hospital, Strasbourg, France
Contact Yvon RUCH, MD
Phone 33 3 69 55 12 19
Email yvon.ruch@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Modification of the rendering of the antibiogram at the Strasbourg University Hospital in November 2019 with the appearance of the concept of "standard dose" or "high dose" sensitivity. This modification seems to have favored an inappropriate overprescription of Meropenem (the only antibiotic made "at standard dose") in Pseudomonas infections sensitive to other beta-lactams. In June 2021, it was therefore decided to mask sensitivity to carbapenems by default in the rendering of Pseudomonas antibiograms when the strain was sensitive to a narrower spectrum beta-lactam ("restricted" antibiogram). The aim of this study is to evaluate the impact of these changes in the antibiogram on antibiotic prescriptions.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date March 13, 2024
Est. primary completion date March 2024
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Major subject (=18 years old) - Subject with a positive blood culture result for Pseudomonas spp identified in the microbiology laboratory of Strasbourg University Hospital during the period from June 1, 2018 to November 30, 2022 - Subject not opposing the reuse of their data for the purposes of this research. Exclusion Criteria: - Subject having expressed opposition to participating in the study, - Pseudomonas spp strain resistant to all first-line beta-lactams (Piperacillin-Tazobactam, Ceftazidime, CĂ©fepime and Aztreonam). - Pseudomonas spp strain resistant to Meropenem. - Lack of information on the antibiotic treatment undertaken.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Service des Maladies Infectieuses et Tropicales - CHU de Strasbourg - France Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Proportion of Meropenem prescriptions in Pseudomonas spp bacteraemia susceptible to narrow-spectrum betalactams This study is retrospective, the analysis focuses on the medical records of patients treated at the Strasbourg University Hospital between June 1, 2018 and November 30, 2022. Files analysed retrospectively from June 1, 2018 to November 30, 2022 will be examined
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