Suspended

Ceftazidime-Avibactam Concentrations in Critically Ill Patients with Renal Failure on CVVHDF

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Study Aim

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).

What is being collected

Data Collection

Collected from today forward - Prospective
No Sample Retained
Who is being recruted

Urogenital Diseases+11

+ Bacterial Infections and Mycoses

+ Bacterial Infections

Over 18 Years
+6 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Case-Only

Examining characteristics of individuals with a disease in order to identify genetic or environmental factors contributing to the condition.
Observational
Study Start: March 2017
See protocol details

Summary

Principal SponsorTemple University
Study ContactChristina Rose, Pharm.D.More contacts
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

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.

Official Title: Pharmacokinetics of Ceftazidime-Avibactam in Critically Ill Patients With Renal Failure Requiring Continuous Venovenous Hemodiafiltration
Principal SponsorTemple University
Study ContactChristina Rose, Pharm.D.More contacts
Last updated: January 27, 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

10 patients to be enrolled

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

Case-only

These studies focus only on individuals who have a specific disease. Researchers examine patterns—often genetic or environmental—to uncover what might be linked to the condition.


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.

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

Urogenital DiseasesBacterial Infections and MycosesBacterial InfectionsFemale Urogenital Diseases and Pregnancy ComplicationsInfectionsKidney DiseasesPathologic ProcessesPathological Conditions, Signs and SymptomsUrologic DiseasesCritical IllnessDisease AttributesRenal InsufficiencyFemale Urogenital DiseasesMale Urogenital Diseases

Criteria

3 inclusion criteria required to participate
Adults > 18 years of age

Patients requiring continuous renal replacement therapy (CRRT) due to acute or chronic renal failure

documented or suspected infection requiring a prescription for ceftazidime-avibactam

3 exclusion criteria prevent from participating
Patients on CRRT < 24 hours

Patients on ceftazidime-avibactam < 24 hours

Patients unable to remain on CRRT for 32 hours continuously without clotting

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

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

Recruiting

Temple University Hospital

Philadelphia, United StatesOpen Temple University Hospital in Google Maps
SuspendedOne Study Center