CompletedNot Applicable

Comparison of Perioperative Standard Fluid Management and Goal-Directed Fluid Management

Turkey (Türkiye)60 participantsStarted 2017-10-01

Plain-language summary

To compare the goal-directed fluid therapy based on the data obtained from the hemodynamic monitoring system, which provides continuous CO, SV and SVV measurements through arterial pressure wave with standard fluid therapy in perioperative fluid management of patients undergoing head and neck surgery.

Who can participate

Age range18 Years – 80 Years

SexALL

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Inclusion criteria

✓. Volunteering to participate in the study
✓. ASA classification 1, 2 or 3
✓. The patients who will undergo head and neck surgery

Exclusion criteria

✕. Being under the age of 18 or over the age of 80
✕. Presence of serious cardiac, renal and liver pathology ( ejection fraction\< %35 and/or glomerular filtration rate\< 30ml/kg/min, kreatinin\>2,5mg/dl and/or abnormal liver function test)
✕. The patients who have heart rhythm problems such as atrial fibrillation, sinus tachycardia, ventricular extrasystoles
✕. The patients who have a peripheral arterial disease
✕. Being a morbid obese ( BMI\>40 kg/m2)
✕. the patients who may have considered difficult airway

What they're measuring

Intraoperative fluid balance

Timeframe: during surgery

Trial details

NCT IDNCT04728178

SponsorIstanbul University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2019-01-01

View on ClinicalTrials.gov More Perioperative Fluid Management trials