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Study of Adverse Effects Occuring in Patients Receiving an Antibiotic Treatment With Temocillin (Témocilline)

C

Centre Hospitalier Universitaire, Amiens

Status

Completed

Conditions

Bacterial Infection With One or More Extended Spectrum Betalactamases Remaining Susceptible to Temocillin

Treatments

Drug: Adverse events detection

Study type

Observational

Funder types

Other

Identifiers

NCT03599999
PI2017_843_0003

Details and patient eligibility

About

The Temocillin prescription frequency may be increased in order to reduce the use of carbapenems to reduce the progressive increase in carbapenem resistance observed in recent years. The investigators wish to study the responsibility of Temocillin in the occurrence of adverse effects in patients in the hospital of Amiens receiving a treatment containing this molecule.

Full description

The study "Continuous versus intermittent infusion of temocillin, a directed spectrum penicillin for intensive care patients with nosocomial pneumoniae: stability, compatibility, population pharmacokinetic studies and breakpoint selection, R. De Jongh, et al, 2007 ", the author states that no adverse effects were found following injection of Temocillin. In the study "Temocillin use in England: clinical and microbiological efficacies in infections caused by extentedspectrum and / or derepressed AmpC β-lactamase-producing Enterobacteriaceae, I. Balakrishnan, et al, 2011, the author faced two cases of Clostridium difficile with a positive toxin test. The first patient received three doses of Amoxicillin / clavulanic acid followed by one week's treatment with Temocillin. This one has developed Clostridium difficile diarrhea on the last day of antibiotic treatment. The second patient did not not received Temocillin in the 6 weeks prior to diarrhea but received 8 days of Meropenem just before this diarrhea. In all cases, Temocillin can not be clearly attributed to this adverse effect and no patient developed pseudomembranous colitis.

Enrollment

26 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • documented bacterial infection with one or more extended spectrum betalactamases remaining susceptible to Temocillin

Exclusion criteria

  • History of hypersensitivity to betalactamines (rash,...)
  • Patient participating in another biomedical research on a drug to avoid the risk of interactions drug
  • Grafted patient
  • Immunocompromised patient
  • Dialysis patient (except hemodialysis patient and dialysis patient peritoneal)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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