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Clinical Trials/NCT03396159
NCT03396159CompletedNot Applicable

Validity of Mini Fluid Challenge to Assess Fluid Responsiveness Post Liver Transplantation

Kasr El Aini Hospital1 site in 1 country30 target enrollmentStarted: January 30, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
30
Locations
1
Primary Endpoint
stroke volume

Study Overview

Brief Summary

our study aim to assess the validity of using mini fluid challenge to assess the volaemic status of patients after liver transplantation

Detailed Description

After approval of institutional ethical committee and after informed patient consent, patients fulfilling criteria will be involved. Upon ICU admission, patients will be connected to full monitoring and confirming patient hemodynamic stability and no active bleeding through drains. Patients will be in supine position and baseline readings will be recorded. Fluid responsiveness will be assessed with mini fluid challenge by 150 ml of albumin 5% given over 1 minute. After fluid administration stroke volume (SV) assessed by trans thoracic echo (TTE) and other hemodynamic parameters will be recorded. Remaining 350 ml of albumin 5% will be continued over 14 minute to have total volume given 500 ml. after fluid administration SV and other parameters will be recorded. The fluid challenge will be given intravenously via a specific wide pore venous line. Fluid responsiveness will be defined as an increase in the SV by 15% after the infusion of fluid.

TT Echo Examination:

A single LVOT diameter will be measured for each patient as the distance between the inflection points at the base of the aortic valve cusps from the left parasternal long axis view during systole.

Assuming a circular cross section, the LVOT area will be calculated from the LVOT diameter as:

π X (LVOT diameter/ 2)2 = (LVOT diameter)2 X 0.785 Pulse wave Doppler sampling cursor will be placed in the middle of the LVOT immediately proximal to the aortic valve in 5 chamber apical view.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients post liver transplantation.
  • ASA III- IV
  • Age > 18 years

Exclusion Criteria

  • Age less than 18 years.
  • Patient with fulminant liver failure.

Arms & Interventions

mini fluid challenge

Experimental

mini fluid will be given and stroke volume will be assessed before and after

Intervention: mini fluid challenge (Diagnostic Test)

Outcomes

Primary Outcomes

stroke volume

Time Frame: 1 minute after mini fluid administration

assessed by trans thoracic echo

Secondary Outcomes

  • heart rate(baseline 10 minutes after intensive care admission, 1 minute after mini fluid challenge and 1 minute after 500 ml of fluid administration)
  • stroke volume(baseline 10 minutes after intensive care admission and 1 minute after 500 ml of fluid administration)
  • mean arterial blood pressure(baseline 10 minutes after intensive care admission and 1 minute after 500 ml of fluid administration)

Investigators

Sponsor
Kasr El Aini Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mohamed Elayashy Mohamed Ahmed Hassan

lecturer of anesthesia

Kasr El Aini Hospital

Study Sites (1)

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