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Clinical Trials/NCT05361252
NCT05361252
Completed
Not Applicable

Restrictive Versus Liberal Stroke Volume Variation-guided Fluid Infusion in Major Liver Tumour Resection: a Prospective Randomised Trial of Perioperative Quality of Care

Kaohsiung Veterans General Hospital.1 site in 1 country118 target enrollmentFebruary 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Fluid Management
Sponsor
Kaohsiung Veterans General Hospital.
Enrollment
118
Locations
1
Primary Endpoint
The incidence of postoperative complications in the two groups.
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Studies have demonstrated that the rate of change in stroke volume variation (SVV) can be used to determine the volume of body fluids during major abdominal surgery. Anaesthesiologists can use SVV as a guide for the appropriate administration of intraoperative fluids to improve postoperative prognoses. Liver surgery is a major abdominal operation, and the amount of blood lost is typically higher than that during other general abdominal surgeries. Blood loss is positively correlated with the intraoperative fluid infusion volume, and greater blood loss is associated with more postoperative complications. Additionally, comorbid liver disease or cirrhosis can increase the complexity of liver tumour resection, causing difficulty in assessing intravascular volume and determining the appropriate intraoperative infusion volume.

Registry
clinicaltrials.gov
Start Date
February 1, 2017
End Date
December 31, 2018
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Yuan-Yi Chia

Chief of Anesthesiology

Kaohsiung Veterans General Hospital.

Eligibility Criteria

Inclusion Criteria

  • We initially selected 118 patients who required hepatectomy.
  • The physiological status of the patients was assessed in terms of American Society of Anesthesiologists scores I-III

Exclusion Criteria

  • Extreme body mass index (BMI)
  • Age under 20 or over 75 years
  • Emergency surgery
  • Preexisting cardiac, hepatic, renal, or coagulation disorder; hyperthyroidism; and sinus arrhythmia.

Outcomes

Primary Outcomes

The incidence of postoperative complications in the two groups.

Time Frame: From day 1 to day 30 after surgery.

calculate the incidence of postoperative complication within 30 days

Secondary Outcomes

  • The differences of perioperative ALT(Examination report on the 1st postoperative day.)
  • The differences of perioperative T.bil(Examination report on the 1st postoperative day.)
  • The differences of perioperative arterial lactate(Examination report on the 1st postoperative day.)
  • The differences of perioperative albumin(Examination report on the 1st postoperative day.)
  • The differences of perioperative creatinine(Examination report on the 1st postoperative day.)
  • The differences of perioperative Hb(Examination report on the 1st postoperative day.)
  • The pain scale(up to three days postoperatively)
  • The differences of perioperative eGFR(Examination report on the 1st postoperative day.)

Study Sites (1)

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