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Clinical Trials/NCT06101498
NCT06101498
Completed
Not Applicable

The Effect of Peroperative Fluid Management Strategy on Postoperative Renal Functions in Major Gyneco-oncological Surgeries

Bakirkoy Dr. Sadi Konuk Research and Training Hospital1 site in 1 country180 target enrollmentJanuary 1, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Fluid Overload
Sponsor
Bakirkoy Dr. Sadi Konuk Research and Training Hospital
Enrollment
180
Locations
1
Primary Endpoint
Evaluation of acute kidney injury
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The aim of this study is to evaluate the effect of perioperative fluid management on postoperative kidney damage in gynecological cancer surgeries.

The main question[s] it aims to answer are:

Does fluid management applied with different hemodynamic monitoring methods affect the risk of postoperative AKI? In our clinic, three different fluid management strategies are applied depending on the anesthetist experience. Acute kidney injury will be evaluated according to the postoperative AKIN classification of conventional fluid therapy and targeted fluid therapy with noninvasive or minimally invasive monitoring.

Detailed Description

Our study was designed as a retrospective study. The files of patients over the age of 18 who underwent open abdominal surgery due to ASAII and III gynecological malignancy will be examined retrospectively. Patients who cannot be monitored peroperatively and who undergo HIPEC will be excluded from the study. Patients will be divided into 3 groups according to the fluid management strategy and the hemodynamic monitoring used: Group 1: patients receiving conventional fluid therapy; Group 2: patients receiving targeted fluid therapy with noninvasive monitoring; Group 3: patients receiving targeted fluid therapy with minimally invasive monitoring.

Registry
clinicaltrials.gov
Start Date
January 1, 2023
End Date
September 1, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Bakirkoy Dr. Sadi Konuk Research and Training Hospital
Responsible Party
Principal Investigator
Principal Investigator

Duygu Akyol

Principal investigator

Bakirkoy Dr. Sadi Konuk Research and Training Hospital

Eligibility Criteria

Inclusion Criteria

  • \>18 years
  • ASA II-III
  • Those with normal renal function

Exclusion Criteria

  • Patients in renal insufficiency
  • Patients with perioperative renal, ureter \& bladder invasion
  • Patients in whom perioperative urine monitoring cannot be performed
  • Patients undergoing HIPEC
  • Patients with missing data

Outcomes

Primary Outcomes

Evaluation of acute kidney injury

Time Frame: Change from preoperative to postoperative day 1(POD1)creatinine values(mg/dl)

Our primary aim was to evaluate the postoperative day(POD1 ) creatinine values(mg/dl)

Secondary Outcomes

  • Peroperative fluid amounts(during the operation period)

Study Sites (1)

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