Completed

Meropenem Pharmacokinetics in Critically Ill Patients Undergoing High-dose Continuous Renal Replacement Therapy

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Study Aim

This study aims to observe the plasma concentration of meropenem in critically ill patients who are undergoing high-dose continuous renal replacement therapy.

What is being collected

Data Collection

Collected from today forward - Prospective
DNA Samples
Who is being recruted

Urogenital Diseases+5

+ Female Urogenital Diseases and Pregnancy Complications

+ Infections

From 18 to 80 Years
+6 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Case-Control

Comparing exposures between individuals with and without disease in order to identify potential risk factors.
Observational
Study Start: April 2018
See protocol details

Summary

Principal SponsorMedical University of Lublin
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: April 2, 2018

Actual date on which the first participant was enrolled.

This study focuses on critically ill patients who have a severe infection and require a specific antibiotic called meropenem, along with a treatment known as Continuous Renal Replacement Therapy (CRRT). The goal is to understand how meropenem works in the body under these conditions. Any patient, whether they're receiving medical or surgical care, can be included, and the type of infection doesn't matter. The importance of this study lies in its potential to improve the use of meropenem in critically ill patients, ensuring they receive the right dose at the right time. During the study, patients receive meropenem through an intravenous (IV) infusion every 8 hours. To understand how the body processes meropenem, small blood samples are collected at various time points after each dose, for 3 consecutive days. These samples are processed and the amount of meropenem in the blood is measured using a specialized technique called high-performance liquid chromatography. Additionally, each patient's health status is closely monitored using a method called transpulmonary thermodilution (PICCO). Other necessary treatments, like ventilatory support or sedation, are provided as needed.

Official TitlePharmacokinetics of Meropenem During High-dose Continuous Renal Replacement Therapy in Critically Ill Patients
NCT03507751
Principal SponsorMedical University of Lublin
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

19 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Case-Control

These studies compare people who have a disease (cases) with those who don't (controls). The goal is to look back at previous exposures or risk factors to identify what might have contributed to the disease.


Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 80 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsInfectionsKidney DiseasesUrologic DiseasesRenal InsufficiencyFemale Urogenital DiseasesMale Urogenital Diseases

Criteria

3 inclusion criteria required to participate
Patients who require ICU treatment due to severe infection

age 18-80 years

an eligible consent obtained from the patient or his/her attendant

3 exclusion criteria prevent from participating
allergy to meropenem

lack of consent to participate in the study

age of patients below 18 or above 80 years

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Oddział Kliniczny Anestezjologii i Intensywnej Terapii, Wojewódzki Szpital Specjalistyczny w Olsztynie

Olsztyn, PolandOpen Oddział Kliniczny Anestezjologii i Intensywnej Terapii, Wojewódzki Szpital Specjalistyczny w Olsztynie in Google Maps
CompletedOne Study Center