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Crystalloids or Colloids for Goal-directed Fluid Therapy With Closed-loop Assistance in Major Surgery

Phase IV, Multicentric, Prospective, Controlled, Randomized, Double Blind Study Comparing a Crystalloid to a Colloid Used in the Perioperatory Hemodynamic Optimisation With a 'Closed Loop' Automatic Filling System, on the Post-surgery Morbidity in Major Abdominal Surgery.

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02312999
Enrollment
160
Registered
2014-12-09
Start date
2015-02-24
Completion date
2017-12-21
Last updated
2018-01-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Surgery

Keywords

laparotomy, plasma-Lyte, volulyte, close loop, abdominal surgery

Brief summary

Study goal: This study will examine whether there is a significant difference in postoperative outcomes between GDFT using a colloid solution versus a crystalloid solution. Hypothesis: Perioperative fluid optimization through the use of a closed-loop assistance with a balanced starch solution (volulyte®) will be associated with a decrease in postoperative complications compared to the same approach using a balanced crystalloid solution (Plasmalyte®). Objective: To establish which kind of intravenous fluid used for goal directed therapy with closed-loop assistance will reduce the number of postoperative complications (evaluation made by the POMS score).

Detailed description

Controversy still persists regarding the type of fluid to use in the operating room to avoid hypovolemia and any circulatory insufficiency. While crystalloids and colloid solutions are frequently used to optimize intravascular volume during surgery, crystalloid solutions require more volume for hemodynamic optimization which may result in higher volumes of fluid administration and potentially side effects. Compared with crystalloids, colloids have the advantages of remaining in the intravascular space longer, achieving faster circulatory stabilization, maintaining colloid osmotic pressure and increasing micro perfusion. However, colloids are more expensive and may have various side effects. In addition to the effect of crystalloids and colloids on the patient, the amount of each fluid administered is also under debate. Goal-directed fluid therapy (GDFT) strategies based on cardiac output (CO) optimization have been shown to benefit moderate- to high-risk surgery patients and have recently been recommended by professional societies in the UK, in France, and in Europe. However, despite the growing evidence, these strategies are often not implemented in current practice. One of the reasons for this lack of implementation is that GDFT strategies, like any other complex clinical protocol, require significant provider attention and vigilance for consistent implementation and it is well known that even under study conditions protocol compliance rates are often not greater than 50% In another hand, one of the chief complicating factors in fluid administration studies is variation in provider administration practices, even when attempting to follow a protocol. Previous studies have used closed-loop (automated) systems to deliver fluid by a standardized protocol, removing variation between providers as one of the confounders of the study. Dr. Cannesson and Rinehart (UC Irvine, California, USA) have recently developed and used a closed-loop system for the provision of GDFT in clinical studies at UC Irvine and La Pitie hospital in France. The closed-loop system is beneficial because it involves the standardization of fluid management and all patients are treated equivalently. This system will thus provide consistent GDFT for all cases in the protocol and remove inter-provider variability as a confounder between groups. Study goal: This study will examine whether there is a significant difference in postoperative outcomes between GDFT using a colloid solution versus a crystalloid solution. Hypothesis: Perioperative fluid optimization through the use of a closed-loop assistance with a balanced starch solution (volulyte®) will be associated with a decrease in postoperative complications compared to the same approach using a balanced crystalloid solution (Plasmalyte®). Objective: To establish which kind of intravenous fluid used for goal directed therapy with closed-loop assistance will reduce the number of postoperative complications (evaluation made by the POMS score).

Interventions

Sponsors

Brugmann University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult patients (over the age of 18) undergoing elective major abdominal surgery that is expected to take longer than 3 hours and requiring a general anesthesia and a minimally invasive cardiac output monitoring (Vigileo/Flotrac) * Patients who provide written informed consent

Exclusion criteria

* Patients under 18 years of age * Patients not undergoing surgery, requiring anesthesia, or cardiac output monitoring * Patients with arrhythmia and/or atrial fibrillation * Patients who are allergic to HES * Patients with renal insufficiency (serum creatinine of \>2 mg/ml) or hepatic dysfunction (liver enzymes \>1.5) * Patients who has coagulation disorders (please define: values higher than 1.5x normal values * Patients without the capacity to give written informed consent or refusal of consent * Patients included in another protocol within a period of 3 months or Participating in another randomised trial * Pregnancy at time of enrolment.

Design outcomes

Primary

MeasureTime frameDescription
POMS score48 hoursDifference between the 2 groups in postoperative morbidity identified with the Post-Operative Morbidity Survey (POMS score) on postoperative days 2.

Secondary

MeasureTime frameDescription
Length of hospitalisationevery day up to 90 days after hospitalisationDifference in duration of hospital length of stay as well as ICU length of stay.
Quantity of fluid administered during surgery24 hoursFluid balance during surgery
Transfusion rate8 daysDifferences of transfusion rate between the two groups, in ml
Hypotension incidence8 daysIncidence of hypotension (defined as total case time spent with 20% drop from baseline preoperative blood pressure).
Need of vasopressors24 hoursDifference in the need and quantity of vasopressors between the two groups
Mortality rate30 daysDifference in 30-day post-operative mortality between the 2 groups
Whodas scale6 months after surgeryEnrolled patients will be contacted by phone and their quality of life assessed by the Whodas scale
Pruritus apparition6 months after surgeryEnrolled patients will be contacted by phone 6 months after surgery and any pruritus apparition will be recorded
Renal function - urea level6 months after surgeryUrea levels. Measured in a blood sample taken according to the standard of care outpatient post-operative follow appointments.
Renal function - creatinine level6 months after surgeryCreatinine levels. Measured in a blood sample taken according to the standard of care outpatient post-operative follow appointments.
Renal function - Estimated glomerular filtration rate (eGFR)6 months after surgeryCreatinine levels. Measured in a blood sample taken according to the standard of care outpatient post-operative follow appointments.
Mean case cardiac index (L /BSA)24 hoursMean case cardiac index (L /BSA), Mean case cardiac stroke volume index (mL/ BSA).

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026