Pure Global

Inferior Vena Cava Compliance in Trans-thoracic Echocardiography: is the Trans-hepatic Window as Reliable as the Subcostal One - Trial NCT04866095

Access comprehensive clinical trial information for NCT04866095 through Pure Global AI's free database. This phase not specified trial is sponsored by Brugmann University Hospital and is currently Completed. The study focuses on Surgical Procedure, Unspecified. Target enrollment is 53 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

Free Database
Powered by Pure Global AI
840K+ Trials
Device Trial
NCT04866095
Completed
Device Trial
device
Trial Details
ClinicalTrials.gov โ€ข NCT04866095
View on ClinicalTrials.gov
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Inferior Vena Cava Compliance in Trans-thoracic Echocardiography: is the Trans-hepatic Window as Reliable as the Subcostal One

Study Focus

Transthoracic echocardiogram

Interventional

device

Sponsor & Location

Brugmann University Hospital

Brussels, Belgium

Timeline & Enrollment

N/A

Jun 25, 2021

Nov 09, 2021

53 participants

Primary Outcome

Difference of sensitivity between the trans-hepatic window versus the subcostal window with TTE,Difference of specificity between the trans-hepatic window versus the subcostal window with TTE

Summary

The ability to assess intravascular volume is an essential part of perioperative care:
 insufficient intravascular volume can result in decreased oxygen delivery to tissues and
 organ dysfunction, while fluid overload can contribute to the development of oedema, organ
 dysfunction, respiratory failure and healing defect.
 
 At the present state, there are many different methods of interpreting intravascular
 circulating blood volume. Non-invasive techniques such as the Clear Sight System, and the
 transthoracic echocardiogram (TTE) have been proposed as non-invasive methods to assess
 patient' blood volume.
 
 The aim of this study is to assess whether the measure of the inferior vena cava (IVC) in the
 trans-hepatic window is as reliable as in the subcostal window to determine fluid
 responsiveness in perioperative patients. In this study, preload increase will be obtained
 through passive leg raising. Sensibility and specificity of the two echocardiographic
 approaches to predict fluid responsiveness will be compared while using the subcostal window
 as the gold standard. The effect of passive leg elevation on patient's cardiac output
 response will be assessed with two different non-invasive techniques: the Clear Sight system
 and the TTE.

ICD-10 Classifications

Surgical procedure, unspecified
Medical procedure, unspecified
Other surgical procedures
During unspecified surgical and medical care
During unspecified surgical and medical care

Data Source

ClinicalTrials.gov

NCT04866095

Device Trial