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Peroperative Fluid Management in Major Gynecological Cancer Surgeries

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06101498
Enrollment
180
Registered
2023-10-26
Start date
2023-01-01
Completion date
2023-09-01
Last updated
2023-11-27

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

Conditions

Acute Kidney Injury, Fluid Loss, Fluid Overload, Perioperative/Postoperative Complications

Keywords

akut kidney injury, goal directed fluid therapy, peroperative fluid management, conventional fluid therapy

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.

Interventions

DIAGNOSTIC_TESTAkut kidnet injury(AKI)

postoperative 24 hours

Sponsors

Bakirkoy Dr. Sadi Konuk Research and Training Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Evaluation of acute kidney injuryChange 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

MeasureTime frameDescription
Peroperative fluid amountsduring the operation periodThe seconder aim to investigate the amount of fluid used peroperatively

Other

MeasureTime frameDescription
The intensive care unit admissionposoperatively up to 1 monthsThe other aim to investigate the intensive care unit admission
Length of staypostoperative 30 daysThe other aim to evaluate the duration of hospital stay.

Countries

Turkey (Türkiye)

Outcome results

None listed

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