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NCT Number: NCT06319677

PK/PD Study of Anti-Infective Drugs in Critically Ill Patients Receiving Extracorporeal Membrane Oxygenation Treatment

Extracorporeal membrane pulmonary oxygenation (ECMO) may provide partial or complete support for organ replacement in patients with severe cardiopulmonary failure, buying time for further management of the primary disease. However, ECMO may significantly alter the pharmacokinetic and pharmacodynamic profiles of critically ill patients, affecting the safety and efficacy of drug therapy. This prospective observational study aims to investigate the impact of ECMO treatment on the pharmacokinetics and pharmacodynamics of antimicrobial drugs in critically ill adult patients. Investigators intend to establish a Population Pharmacokinetic (POP PK) and Pharmacokinetic/Pharmacodynamic (PK/PD) model by prospectively collecting blood samples from patients and relevant treatment data. The primary objective is to quantitatively characterize the pharmacokinetic profiles of critically ill patients undergoing ECMO support and provide model-based recommendations for drug regimens tailored to critically ill patients.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

Extracorporeal Membrane Pulmonary Oxygenation (ECMO) is a temporary life-support system used to provide partial or complete organ support for adult patients with severe cardiopulmonary failure. ECMO stabilizes the vital signs of critically ill patients, allowing time for further management of the underlying disease. Effective pharmacologic treatment of the primary condition is crucial for successful patient outcomes.

Critically ill patients often exhibit significant variability in pharmacokinetics (PK) compared to the general population. Moreover, the use of extracorporeal therapeutic techniques like ECMO introduces further variability and unpredictability in drug behavior. This can result from factors such as drug depletion within ECMO circuits, altered drug distribution volumes, and reduced drug excretion.

Sepsis and septic shock due to infections like pneumonia are life-threatening conditions frequently requiring admission to intensive care units. Timely and effective antimicrobial therapy is vital to reduce morbidity and mortality. To investigate the impact of ECMO therapy on the PK and PD of antimicrobial drugs, this prospective observational study will collect blood samples from critically ill adult patients, both those receiving ECMO treatment and those not receiving it. The study will focus on various antimicrobial agents, including imipenem, vancomycin, piperacillin/tazobactam, ceftazidime/avibactam, cefoperazone/sulbactam, cefepime, ceftriaxone, ticlopidine, linezolid, tigecycline, amikacin, gentamicin, polymyxin, voriconazole, fluconazole, caspofungin, micafungin, levofloxacin, and moxifloxacin. Data collected will be used to develop a Population Pharmacokinetic and Pharmacodynamic model based on patient demographics, laboratory results, dosing information, and blood concentration data.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Written informed consent was obtained from the patient or family member
  • Patients who are undergoing ECMO or not
  • Anti-infection treatment indications

Exclusion criteria

  • Patients under 18 years of age or pregnant
  • Information on antimicrobial therapy and ECMO support is incomplete
  • Presence of other circumstances that make participation in this study inappropriate

Treatment and study plan

ECMO treatment

Device

Critically ill patients were treated with ECMO while receiving antimicrobial therapy

Primary outcomes

  1. Blood drug concentration

    Time frame: Samples were taken in the first 72 hours after administration according to the sampling schedule

    Plasma drug concentration

  2. Pharmacokinetic parameter

    Time frame: 24 hours after administration

    Area under the plasma concentration-time curve(AUC)

  3. Pharmacokinetic parameter

    Time frame: 12 hours after administration

    Peak Plasma Concentration (Cmax)

Secondary outcomes

  1. Mortality at 14 and 28 days

    Time frame: Day 30 of the patient's admission

    Mortality was measured by dividing the number of subjects who died during the observation period by the total number of subjects and multiplying by 100%.

Study contacts

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

Jingjing Liu, Doctor

CONTACT

[email protected]

+86 0731-88618170

Shengnan Zhang

CONTACT

[email protected]

+86 18084668240

Sponsors and collaborators

Lead sponsor

The Third Xiangya Hospital of Central South University

Other

Registry information

Official study title

PK/PD Study of Antibiotics in Critically Ill Patients Receiving ECMO

Acronym: ECMO

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Mar 20, 2024
Registry last updated
Mar 20, 2024

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.

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