Clinical Trial

Risk Factors for AKI in Patients Undergoing VATS for Pulmonary Resection

Recruiting
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Record status
This record was last updated January 30, 2025 (before its estimated July 15, 2025 completion). Its status may not reflect the trial's current state.
Summary
This study aims to investigate the potential factors contributing to the development of Acute Kidney Injury (AKI) in patients undergoing pulmonary resection with Video Assisted Thoracoscopic Surgery (VATS) for lung malignancy. The study will focus on demographic data, laboratory parameters, perioperative fluid management, and haemodynamics. The research will be conducted at SBÜ Ankara Atatürk Sanatorium Training and Research Hospital. The study will involve patients who have given informed consent and will undergo VATS with standard anaesthesia monitoring. Anaesthesia management will follow our routine protocol in our clinic. Patients will be divided into two groups based on whether they have a more than 25% decrease in estimated glomerular filtration rate (t-GFH) and/or a 1.5-fold increase in serum creatinine and/or a 6-hour urine volume of less than 0.5 ml/kg/h. The patients will be divided into two groups based on this definition, and the risk factors between these groups will be analysed. The preoperative routine blood values, demographic data (age, gender, height, weight, and BMI), ASA physical status, smoking and alcohol habits, comorbidities, and regular medication use will be recorded. Intraoperative urine output and haemodynamic parameters will also be monitored. Routine blood gas analysis, blood urea nitrogen (BUN), glomerular filtration rate (GFR), albumin, haemoglobin, sodium, potassium, chlorine, and magnesium will be measured and recorded, along with urine output and t-GFH. Patients will be evaluated in the hospital on the day the surgeon calls for a postoperative check-up and on the 30th postoperative day to see if there are any complications.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2024-03-26.
Status change: Not Yet Recruiting → Recruiting 2025-01-28
Trial Details
NCT Number NCT06341933
Lead Sponsor Atatürk Chest Diseases and Chest Surgery Training and Research Hospital
Conditions Acute Kidney Injury, Surgery, Lung Cancer
Enrollment 100 participants
Start Date 2024-04-15
Primary Completion 2025-07-15 (estimated)
Study Completion 2025-12-15 (estimated)
Updated on ClinicalTrials.gov 2025-01-30