Meropenem Pharmacokinetics in Critically Ill Patients Undergoing High-dose Continuous Renal Replacement Therapy
This study aims to observe the plasma concentration of meropenem in critically ill patients who are undergoing high-dose continuous renal replacement therapy.
Data Collection
Collected from today forward - ProspectiveUrogenital Diseases+5
+ Female Urogenital Diseases and Pregnancy Complications
+ Infections
Case-Control
Comparing exposures between individuals with and without disease in order to identify potential risk factors.Summary
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.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.19 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Case-Control
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.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
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.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
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