Clinical Trials Directory

Trials / Completed

CompletedNCT06729268

Fluid Responsiveness Tests in Critically Ill Patients During Admission to the Intensive Care Unit

Possibility of Applying Fluid Responsiveness Tests in Critically Ill Patients During Admission to the Intensive Care Unit - a Prospective Observational Study.

Status
Completed
Phase
Study type
Observational
Enrollment
389 (actual)
Sponsor
Uniwersytecki Szpital Kliniczny w Opolu · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this observational study is to investigate the prevalence of conditions allowing the performance fluid responsiveness tests in critically ill patients during admission to the intensive care unit.

Detailed description

Patients admitted to the intensive care unit are very often hemodynamically unstable. In these cases fluid responsiveness tests should be performed to assess whether the patient would benefit from the fluid administration. However, fluid responsiveness tests have many limitations including lack of spontaneous breathing, necessity of invasive mechanical ventilation with tidal volume of \> 8 mL/kg ideal body weight, regular hearth rhythm, and lack of abdominal hypertension. In the study, the investigators evaluated the prevalence of conditions enabling the performance fluid responsiveness tests in patients admitted to the intensive care unit. An assessment was performed within the six hours after admission to the intensive care unit. Evaluation was based on transthoracic echocardiography, clinical examination of the patients, and data derived from anamnesis. The following fluid responsiveness tests were included into assessment: passive leg raising test, end-expiratory occlusion test, pulse pressure variation, stroke volume variation, velocity time integral variation in left ventricle output track, tidal volume challenge, inferior vena cava diameter variation, and superior vena cava diameter variation. The aim of the study was to assess how many patients have the conditions allowing performance fluid responsiveness tests during admission to the intensive care unit.

Conditions

Timeline

Start date
2023-04-03
Primary completion
2024-05-27
Completion
2024-05-27
First posted
2024-12-11
Last updated
2024-12-31

Locations

1 site across 1 country: Poland

Source: ClinicalTrials.gov record NCT06729268. Inclusion in this directory is not an endorsement.