Viewing Study NCT04732481



Ignite Creation Date: 2024-05-06 @ 3:44 PM
Last Modification Date: 2024-10-26 @ 1:55 PM
Study NCT ID: NCT04732481
Status: COMPLETED
Last Update Posted: 2022-03-09
First Post: 2021-01-27

Brief Title: Evaluation of Corrected Carotid Flow Time Variations During Passive Leg Lift to Predict Response to Filling
Sponsor: Centre Hospitalier de Cornouaille
Organization: Centre Hospitalier de Cornouaille

Study Overview

Official Title: Evaluation of Corrected Carotid Flow Time Variations During Passive Leg Lift to Predict Response to Filling
Status: COMPLETED
Status Verified Date: 2022-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: CAROT
Brief Summary: Patients hospitalized in intensive care often require intravenous administration of fluid in order to optimize the functioning of the heart and thus ensure perfusion of vital organs such as the kidneys the brain or the digestive tract However it is necessary to find the right balance in fluid intake because it has been shown that excessive administration has a negative impact on patient survival the length of their stay in intensive care or the duration of invasive mechanical ventilationThe passive leg lifting maneuver is regularly used to determine which patients should be infused with these large volumes the patients chest is placed in a horizontal position and the legs are elevated at 30 by tilting the bed for 2 minutes To be interpreted this maneuver requires the presence of invasive devices bloody arterial pressure catheter PICCO monitor or an operator experienced in cardiac ultrasoundOur study aims to evaluate an easy-to-use non-invasive tool widely available in intensive care and emergency departments carotid vascular doppler ultrasound to assess the response to a passive leg lifting maneuver The measurements are taken before and after a passive leg lifting maneuver and then before and after a filling decided before inclusion by the doctor responsible for the patient
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None