Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID05606536

The Impact of Intra-operative Fluid Infusion Rate on Hemodilution and Microcirculation Prospective Observational Pilot Study

Led by University Hospital Hradec Kralove · Updated on 2025-03-27

80

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating the impact of different rates of intraoperative fluid therapy (IFT) on microcirculation and hemodilution during elective recumbent and laparoscopic surgeries. IFT is used to optimize oxygen delivery to tissues during surgery, but the optimal fluid dosage remains unclear. Surgery can damage the endothelial glycocalyx (EG), a key structure affecting microcirculation and tissue metabolism, leading to plasma release and hemodilution. This study aims to understand how IFT affects microcirculation parameters and postoperative outcomes. The study compares several infusion rates of crystalloid solutions based on the type of surgery. For recumbent and laparoscopic surgeries, different infusion rates are given during the first 20 minutes followed by a reduced rate thereafter. The study includes experimental groups with 10%, 20%, and 30% hemodilution, as well as a standard care group. The fluid infusion is tailored by weight (ml/kg/h) and administered during surgery to observe its effects. Participants will undergo their planned surgery with assigned fluid infusion rates. Researchers will measure sublingual microcirculation profiles one hour after fluid administration as the primary outcome. The study monitors blood loss and hemodynamic stability during surgery. Participation involves elective surgery and fluid management with no masking or randomization. The trial started in October 2022 and is expected to end in December 2025.

CONDITIONS

Brief 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 or laparoscopic surgery
  • Provided informed consent
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Duration of the surgery

Participants receive intraoperative fluid infusion at predefined rates during elective recumbent or laparoscopic surgery to evaluate the impact on microcirculation.

1 visit (during surgery)

Follow-up

Duration - 1 hour

Participants are observed for changes in sublingual microcirculation profile for 1 hour after surgery.

1 post-operative visit

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

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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