Ignite Creation Date:
2024-06-16 @ 11:51 AM
Last Modification Date:
2024-10-26 @ 3:31 PM
Study NCT ID:
NCT06440772
Status:
COMPLETED
Last Update Posted:
2024-06-04
First Post:
2024-05-30
Brief Title:
Portal Vein Pulsatility Index to Assess Fluid Intolerance
Sponsor:
Institutul de Urgenţă pentru Boli Cardiovasculare ProfDr CC Iliescu
Organization:
Institutul de Urgenţă pentru Boli Cardiovasculare ProfDr CC Iliescu
Study Overview
Official Title:
Assessing Fluid Intolerance Using Portal Vein Pulsatility Index Post-Passive Leg Raising Test in Fluid Responders A Prospective Cohort Study
Status:
COMPLETED
Status Verified Date:
2024-08
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:
None
Brief Summary:
This study uses the portal vein pulsatility index PVPI to assess fluid intolerance amongst fluid responders
Detailed Description:
This prospective observational study aims to use the portal vein pulsatility index PVPI to assess fluid intolerance in fluid responders The investigators will enroll mechanically ventilated postoperative adult patients within 6 hours of ICU admission after cardiac surgery Patients will undergo a Passive Leg Raising PLR test and Left Ventricular Outflow Tract LVOT recording using transthoracic echocardiography The main objective is to predict fluid intolerance after a fluid challenge of 7 mlkg Ringer Lactate over 10 minutes in initially tolerant fluid responders
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