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Validity of Mini Fluid Challenge Post Liver Transplantation

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03396159
Enrollment
30
Registered
2018-01-10
Start date
2018-01-30
Completion date
2018-05-20
Last updated
2018-07-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Liver Transplantation

Keywords

liver transplantation, mini fluid challenge

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. The sonographer manually will trace the velocity-time envelope (VTI). SV values will be calculated by multiplying VTI by cross sectional area.

Interventions

DIAGNOSTIC_TESTmini fluid challenge

mini fluid challenge will be given to diagnose if patient is need fluid resuscitation or not

Sponsors

Kasr El Aini Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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.

Design outcomes

Primary

MeasureTime frameDescription
stroke volume1 minute after mini fluid administrationassessed by trans thoracic echo

Secondary

MeasureTime frameDescription
heart ratebaseline 10 minutes after intensive care admission, 1 minute after mini fluid challenge and 1 minute after 500 ml of fluid administration
stroke volumebaseline 10 minutes after intensive care admission and 1 minute after 500 ml of fluid administrationassessed by trans thoracic echo
mean arterial blood pressurebaseline 10 minutes after intensive care admission and 1 minute after 500 ml of fluid administration

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026