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NCT Number: NCT07287813

Extracorporeal Therapy and Therapeutic Drug Monitoring

The aim of this study is to comparatively evaluate serum concentrations of continuously applied antibiotics in ICU patients, with and without ECMO/RRT support.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

Among all patients being treated with new generation antibiotics (beta.lactams and beta-lactamase inhibitors), we will take into consideration the results of those admitted to intensive care units.

Effective antimicrobial treatment is critical to reduce their mortality associated with bacterial sepsis. They often also require extracorporeal supports, such as renal replacement therapy (RRT) and extracorporeal membrane oxygenation (ECMO), for their survival. However, few studies, limited only to some drugs, report the importance of therapeutic drug monitoring for adequate dose adjustment in these particular conditions of extracoporeal support.

The risk of reaching sub therapeutic or toxic levels is quite high, due to possible very significant variations in the pharmacokinetics of the drugs because of their interaction with the various components of the ECMO and RRT devices, the characteristics of the drug itself and the pathophysiological changes of the patients on ECMO and/or RRT.

Primary aim is to evaluate whether the standard prescriptions of beta lactams/beta lactamase inhibitors (BL/BLIs) are adequate to achieve the optimal PK/PD target also for ECMO and RRT (or combined) patients admitted to intensive care unit.

Secondary aims include to evaluate:

  • the occurrence of sub-therapeutic and/or toxic drugs levels
  • the proportion of patients with insufficient drugs levels in different subgroups (i.e., absence of extracorporeal therapy vs. ECMO; absence of extracorporeal therapy vs. RRT, absence of extracorporeal therapy vs ECMO and RRT) - the proportion of patients with toxic or sub-therapeutic drugs levels in the same subgroups;
  • the proportion, when possible, of drugs level before and during the extracorporeal therapy, for the same patient;
  • the occurrence of drug resistance by pathogens and their mechanism

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • adult patients (age 18y or older)
  • admitted to ICU
  • supported or not-supported with extracorporeal membrane oxygenation (ECMO) and/or renal replacement therapy (RRT)
  • affected by gram-negative bacterial infections susceptible to the novel antibiotics.

Exclusion criteria

  • Pediatric age (<18y)
  • allergies to pharmaceutical and/or inactive drug ingredients (excipients)
  • life expectancy less than 1 month
  • body mass index (BMI) >45 kg/m2
  • pregnancy

Treatment and study plan

Primary outcomes

  1. Primary aim

    Time frame: up to 24 months

    evaluate whether the standard prescriptions of beta lactams/beta lactamase inhibitors (BL/BLIs) are adequate to achieve the optimal PK/PD target also for ECMO and RRT (or combined) patients admitted to intensive care unit.

Secondary outcomes

  1. occurrence of sub-therapeutic and/or toxic drugs levels

    Time frame: up to 24 months

  2. proportion of patients with insufficient drugs levels in different subgroups

    Time frame: up to 24 months

  3. proportion of patients with toxic or sub-therapeutic drugs levels in the same subgroups

    Time frame: up to 24 months

  4. proportion, when possible, of drugs level before and during the extracorporeal therapy, for the same patient

    Time frame: up to 24 months

  5. occurrence of drug resistance by pathogens and their mechanism

    Time frame: up to 24 months

Study contacts

Contact information is provided by the study sponsor or research team.

Simona De Gregori

CONTACT

[email protected]

+39 0382503647

Sponsors and collaborators

Lead sponsor

Fondazione IRCCS Policlinico San Matteo di Pavia

Other

Registry information

Official study title

Pharmacokinetics/Pharmacodynamics and Therapeutic Drug Monitoring of Novel β-lactams and β-lactamase Inhibitors in Critically Ill Patients Undergoing Extracorporeal Therapy

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Dec 17, 2025
Registry last updated
Dec 17, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.