Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- Elective recumbent or laparoscopic surgery
- Provided 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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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)
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
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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