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Defining Antibiotic Levels in Intensive care patients (DALI-2) protocol - A multi-national pharmacokinetic/pharmacodynamic cohort study to determine whether contemporary antibiotic dosing for critically ill patients achieves therapeutic exposures.

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-516232-10-00
Acronym
LOCAL/2024/CR-03
Enrollment
200
Registered
2025-10-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Serious infections in critically ill patients treated with antibiotics

Brief summary

The primary endpoint is the antibiotic PK/PD plasma target defined in Table 1 for each study drug. Antibiotic plasma concentrations will be measured as described in Section 10 of the protocol.

Detailed description

Alternative PK/PD targets: i. 50% fT>MIC, 50% fT>4xMIC, 100%fT>MIC and 100%fT>4xMIC for beta-lactam antibiotics. ii. In adults, a trough concentration of ≥15 mg/L, and 15 to 25 mg/L for vancomycin intermittent and continuous infusions. iii. In children, a trough concentration range of 15 to 20 mg/L for methicillin-resistant Staphylococcus aureus (MRSA) and 10 to 15 mg/L for non-MRSA., Correlation between targeted antibiotic plasma concentrations and i. Clinical success ii. Clinical failure iii. Mortality at day 14 and day 30 after initiation of the study antibiotic. iv. The number of ICU free days at day 30 after initiation of the study antibiotic. v. Identification of resistant organisms in the subsequent microbiological samples within 14 days of study antibiotic start., Proportion of patients whose observed antibiotic concentrations surpass the pre-defined values associated with toxicity, Correlation between antibiotic plasma concentrations and the occurrence of adverse events, Description of observed antibiotic plasma concentrations

Interventions

DRUGLINEZOLID
DRUGMEROPENEM
DRUGLEVOFLOXACIN
DRUGAZTREONAM AND BETA-LACTAMASE INHIBITOR
DRUGCEFTAZIDIME
DRUGCOLISTIN
DRUGAMOXICILLIN
DRUGVANCOMYCIN
DRUGERTAPENEM
DRUGTIGECYCLINE
DRUGIMIPENEM
DRUGFOSFOMYCIN
DRUGTEICOPLANIN
DRUGAMPICILLIN
DRUGGENTAMICIN
DRUGDAPTOMYCIN
DRUGCEFEPIME
DRUGCEFOTAXIME
DRUGCEFTRIAXONE
DRUGTOBRAMYCIN
DRUGCIPROFLOXACIN
DRUGMETRONIDAZOLE
DRUGAMIKACIN
DRUGCEFAZOLIN

Sponsors

Centre Hospitalier Universitaire De Nimes
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
The primary endpoint is the antibiotic PK/PD plasma target defined in Table 1 for each study drug. Antibiotic plasma concentrations will be measured as described in Section 10 of the protocol.

Secondary

MeasureTime frame
Alternative PK/PD targets: i. 50% fT>MIC, 50% fT>4xMIC, 100%fT>MIC and 100%fT>4xMIC for beta-lactam antibiotics. ii. In adults, a trough concentration of ≥15 mg/L, and 15 to 25 mg/L for vancomycin intermittent and continuous infusions. iii. In children, a trough concentration range of 15 to 20 mg/L for methicillin-resistant Staphylococcus aureus (MRSA) and 10 to 15 mg/L for non-MRSA., Correlation between targeted antibiotic plasma concentrations and i. Clinical success ii. Clinical failure iii. Mortality at day 14 and day 30 after initiation of the study antibiotic. iv. The number of ICU free days at day 30 after initiation of the study antibiotic. v. Identification of resistant organisms in the subsequent microbiological samples within 14 days of study antibiotic start., Proportion of patients whose observed antibiotic concentrations surpass the pre-defined values associated with toxicity, Correlation between antibiotic plasma concentrations and the occurrence of adverse events, D

Countries

France

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026