Kasr Alainy Hospital , Faculty of Medicine
Cairo, Egypt
NCT Number: NCT03396159
our study aim to assess the validity of using mini fluid challenge to assess the volaemic status of patients after liver transplantation
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Not applicable
Cairo, Egypt
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
mini fluid challenge will be given to diagnose if patient is need fluid resuscitation or not
Time frame: 1 minute after mini fluid administration
assessed by trans thoracic echo
Time frame: baseline 10 minutes after intensive care admission, 1 minute after mini fluid challenge and 1 minute after 500 ml of fluid administration
Time frame: baseline 10 minutes after intensive care admission and 1 minute after 500 ml of fluid administration
assessed by trans thoracic echo
Time frame: baseline 10 minutes after intensive care admission and 1 minute after 500 ml of fluid administration
Kasr El Aini Hospital
Other
Validity of Mini Fluid Challenge to Assess Fluid Responsiveness Post Liver Transplantation
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07728604
Behavior, Health Behavior
Izmir, Turkey (Türkiye)
View Trial DetailsNCT01294020
Heart Transplantation, Intestine Transplantation
Brussels, Belgium
View Trial DetailsNCT07233083
Liver Transplantation, Neurologic Manifestations
Istanbul, Turkey (Türkiye)
View Trial DetailsNCT07233096
Liver Transplantation, Living Donor
Istanbul, Turkey (Türkiye)
View Trial Details