Non Invasive Evaluation of Fluid Responsiveness in Septic Patient

Status Active, not recruiting

Clinical Trial Summary

The study aims to evaluate the accuracy of fluid responsiveness assessment with non-invasive cardiometry compared to ultrasound guided inferior vena cava (IVC) collapsibility for management of critically ill septic patients with hemodynamic instability.

Clinical Trial Description

Prospective Randomized observational comparative single blinded study will be conducted at intensive care unit at Benha University Hospitals after obtaining approval of the ethical committee and informed written consent from first degree relatives will be issued. The blindness will be performed to the patients. The study will be conducted according to CONSORT 2010 statement. Enrolment of eligible patients will occur within 8 h of meeting the criteria for septic shock. All patients will be randomized using the computer-generated software of randomization and sealed closed envelopes to allocate them to one of two groups (30 patients each). Routine measurements and investigations will be taken at admission to intensive care unit; history, vital signs, routine laboratory investigation. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05310942
Study type	Observational
Source	Benha University
Contact
Status	Active, not recruiting
Phase
Start date	December 17, 2021
Completion date	January 1, 2023

View Details

See also
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