Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05606536

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Elective recumbent and laparoscopic surgery
  • Informed consent
Not Eligible

You will not qualify if you...

  • Blood loss over 250 ml
  • Hemodynamic instability requiring noradrenaline infusion

AI-Screening

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Trial Site Locations

Total: 1 location

1

University Hospital Hradec Kralove

Hradec Králové, Czechia, 50005

Actively Recruiting

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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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