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Clinical Trials/NL-OMON43959
NL-OMON43959
Recruiting
Not Applicable

An exploratory pharmacokinetic and pharmacodynamic study of beta-lactam and fluoroquinolone in ICU patients - EXPAT

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sepsis
Sponsor
Erasmus MC, Universitair Medisch Centrum Rotterdam
Enrollment
200
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • All the patients admitted to the ICU or internal medicine ward and given standard of care intravenous therapy of either one or both of the target antibiotic classes are included. Antibiotic initiation based on clinical suspicion of infection and/or cultured pathogens susceptible to the target drugs, initial dosage prescription, and duration of therapy are at the discretion of the attending physician. ;In order to be eligible to participate in this study, a subject must also meet all of the following criteria:
  • \* Written informed consent has been obtained from the patient or their legally authorized representative.
  • \* Receiving intravenous antibiotic therapy of the target drugs.
  • \* Suitable intravenous/intra\-arterial access to facilitate sample collection.
  • \* Treatment should be aimed for at least at 3 days.
  • \* Bacterial isolates sample are obtainable before start of the target drugs.

Exclusion Criteria

  • \* Consent not obtained.
  • \* \<18 years of age.
  • \* Antibiotic cessation within 72h after start of the therapie.
  • \* Medium care and burn wound patients admitted to the ICU.

Outcomes

Primary Outcomes

Not specified

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