Viewing Study NCT06423833



Ignite Creation Date: 2024-06-16 @ 11:48 AM
Last Modification Date: 2024-10-26 @ 3:30 PM
Study NCT ID: NCT06423833
Status: RECRUITING
Last Update Posted: 2024-05-23
First Post: 2024-05-16

Brief Title: Trendelenburg Maneuver Versus Passive Leg Raising Test for Fluid Responsiveness in High-Risk Surgical Patients
Sponsor: Tanta University
Organization: Tanta University

Study Overview

Official Title: Trendelenburg Maneuver Versus Passive Leg Raising Test for Fluid Responsiveness in High-Risk Surgical Patients
Status: RECRUITING
Status Verified Date: 2024-05
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: The aim of this study is to evaluate whether Trendelenburg maneuver can be used to predict fluid responsiveness in high-risk surgical patients in intensive care unit as compared to Passive Leg Raising test
Detailed Description: Passive Leg Raising test is a well validated dynamic method to predict fluid responsiveness with many advantages as it doesnt use fluid loading its effect is reversible and it doesnt rely on heart-lung interaction However it has many limitations as has false negative effect in patients with intra-abdominal hypertension also it may not be suitable in some surgical patients

Trendelenburg maneuver TM is often used to treat hemodynamic unstable patients when hypovolemia is suspected through a mechanism similar to Passive Leg Raising test Yonis et al reports that change in cardiac output during Trendelenburg maneuver is a reliable predictor of fluid responsiveness in patients with acute respiratory distress syndrome in prone position under protective ventilation Another study reports that change in velocity time integral during trendelenburg maneuver predicts fluid responsiveness in cardiac surgical patients in operating rooms

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