Personalized Antibiotic Therapy - Point-of-Care Determination of Blood Levels of Beta-Lactam Antibiotics Using Coated-Blade-Spray Ion Mobility Spectrometry

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorDr. T. Perl

About this trial

A new analytical method for determining beta-lactam antibiotic concentrations in the blood of intensive care patients is to be evaluated. Patients receive antibiotic therapy with beta-lactam antibiotics in the general surgery intensive care unit. Blood samples are collected daily for routine clinical testing; a portion of these samples is used for the new method. The antibiotic levels, routinely measured using the gold standard, are documented and used as a reference point. The goal of the study is to establish a rapid and cost-effective method for determining beta-lactam antibiotic levels, which will subsequently enable rapid dose adjustment.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Valid informed consent form (prospective, retrospective, or provided by a legal representative)

Antibiotic therapy with a beta-lactam antibiotic in the intensive care unit or intermediate care unit of the Department of General Surgery at UMG

Disqualifiers

Patients without a valid informed consent form

Trial population

Patents that are treated with beta-lactam antibiotics in the ICU or IMC unit of the Department of General Surgery at UMG

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Blood levels of beta-lactam antibiotics

Blood levels of beta-lactam antibiotics are measured both through routine clinical testing and using the newly developed analytical method. Blood samples are collected once a day for this purpose. Changes in blood levels are monitored over several days.

Time frame
Daily, approximately 5-10 days from start of anibiotic therapy (and enrollment) to the end of antibiotic therapy

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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Dr. T. Perl

Lead sponsor

University of Göttingen

Sponsor institution

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