Ceftazidime-Avibactam Concentrations in Critically Ill Patients with Renal Failure on CVVHDF
This observational study aims to measure the concentrations of Ceftazidime-Avibactam in both the plasma and effluent of critically ill patients with renal failure who are undergoing CVVHDF (Continuous Veno-venous Hemodiafiltration).
Data Collection
Collected from today forward - ProspectiveUrogenital Diseases+11
+ Bacterial Infections and Mycoses
+ Bacterial Infections
Case-Only
Examining characteristics of individuals with a disease in order to identify genetic or environmental factors contributing to the condition.Summary
Study start date: March 13, 2017
Actual date on which the first participant was enrolled.This study focuses on critically ill patients with renal failure who need a treatment called continuous venovenous hemodiafiltration (CVVHDF). These patients are also prescribed a medication named Ceftazidime-Avibactam to treat their infection. The main goal is to understand how this drug behaves in their bodies, particularly in the blood and dialysis fluid. The study is important as it helps determine if the usual dose of Ceftazidime-Avibactam is suitable for such patients, potentially improving their care and addressing the challenges associated with their condition. During the study, researchers measure the levels of Ceftazidime-Avibactam in both the patients' blood and the fluid removed during CVVHDF. This helps them evaluate how the drug moves through the body when it's filtering blood. The study assesses if the drug reaches certain targets, which indicate its effectiveness. By examining these concentrations, the study provides insights into the drug's behavior in critically ill patients with renal failure undergoing CVVHDF.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.10 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Case-only
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.Over 18 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
Secondary 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