Actively Recruiting
The Impact of Intra-operative Fluid Infusion Rate on Microcirculation
Led by University Hospital Hradec Kralove · Updated on 2025-03-27
80
Participants Needed
1
Research Sites
169 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Intraoperative fluid therapy (IFT) is an integral part of anesthesia care during surgery. Its main indication is the optimization of oxygen supply to the tissues. For elective surgery that is not associated with higher blood loss and a long period of preoperative fasting, including fluids IFT is dosed to cover the basal daily need for fluids. However, it is not clear whether this fluid dose is optimal. Surgery is a stress factor that leads, among other things, to damage of the endothelial glycocalyx (EG). EG binds a significant amount of plasma, which is released during EG destruction and causes relative hemodilution. Isovolumic hemodilution is an established intraoperative procedure that serves to better control bleeding in procedures where bleeding is expected. However, partial hemodilution occurs even with standard IFT, and even when fluids are hardly given at all. Flow parameters in microcirculation have not yet been described depending on IFT conduction. The parameters of the microcirculation reflect its functioning, which will consequently affect the postoperative phase of the patient's moaning and clinical outcome.
CONDITIONS
Official Title
The Impact of Intra-operative Fluid Infusion Rate on Microcirculation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Elective recumbent and laparoscopic surgery
- Informed consent
You will not qualify if you...
- Blood loss over 250 ml
- Hemodynamic instability requiring noradrenaline infusion
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University Hospital Hradec Kralove
Hradec Králové, Czechia, 50005
Actively Recruiting
Research Team
D
David Astapenko, MD, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
4
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