Ignite Creation Date:
2024-05-06 @ 7:01 PM
Last Modification Date:
2024-10-26 @ 2:58 PM
Study NCT ID:
NCT05862298
Status:
RECRUITING
Last Update Posted:
2024-05-01
First Post:
2023-05-08
Brief Title:
Spinal-Induced Hypotension in Geriatric Patients
Sponsor:
Tanta University
Organization:
Tanta University
Study Overview
Official Title:
Pre-Anaesthetic Venous Excess Ultrasound -Score and Their Correlations With the Spinal-Induced Hypotension in Geriatric Patients
Status:
RECRUITING
Status Verified Date:
2024-04
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 study will be conducted to asses preoperative condition of venous system by VExUS score and its relation with the incidence of spinal induced hypotension in geriatric patients undergoing surgery with spinal anaesthesia
Detailed Description:
An assessment of the intravascular volume deficit prior to the spinal anaesthesia conduction may help to predict the occurrence of a critical decrease in blood pressure so several indices have been proposed to assess its status depending on either a fluid challenge or an assessment of heart-lung interaction Heart rate variability passive leg raise test and peripheral perfusion index have revealed good abilities to predict spinal induced hypotension The inferior vena cava IVC collapsibility index provides high diagnostic accuracy in predicting spinal induced hypotension The VeXUS score is a four-staged validated protocol which evaluates the presence and severity of systemic venous congestion in the inferior vena cava IVC and organs liver gut and kidneys by evaluating the IVC diameter venous waveforms of the hepatic vein HV portal vein PV and interlobar renal veins using colour Doppler CD and pulsed wave Doppler PWD
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