The Impact of Intra-operative Fluid Infusion Rate on Microcirculation

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity Hospital Hradec Kralove

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

elective recumbent and laparoscopic surgery

informed consent

Disqualifiers

blood loss over 250 ml

hemodynamic instability requiring noradrenaline infusion

Trial design

Design model

Parallel

Treatments tested in this trial

  • Crystalloid Solutions

    Drug

    Locally approved crystalloid solution will be given at the predefined infusion rate

Treatment groups

80 Participants
are divided into 4 treatment groups
Group A: 10 % hemodilutionExperimental treatment 1 intervention
Group B: 20 % hemodilutionExperimental treatment 1 intervention
Group C: 30 % hemodilutionExperimental treatment 1 intervention
Group D: Standart careNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Sublingual microcirculation profile

During one hour four measurements each 20 minutes will take place. Recordings will be assessed automatically by specialised software. Microcirculatory parameters of interest are: capillary density, De Backer score, perfused capillary density and proportion of perfused vessels. Capillary density comes in mm/mm2 and the higher number the better, there is not approved median number. De Backer score is derived from capillary density and it is without dimension. Perfused capillary density signifies a percent of perfused vessels and it is in %. Normal values in healthy adults are around 90 %.

Time frame
1 hour

Secondary outcomes

Other outcomes

Sponsors and contacts

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