Clinical Trial

Assessment of Renal Perfusion Using Ultrasound and Near-Infrared Spectroscopy in Patients Undergoing Minimally Invasive Abdominal Surgery

Study acronym: RRI-NIRS
Recruiting
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Summary
This prospective observational study aims to evaluate renal perfusion in adult patients undergoing elective minimally invasive abdominal surgery. Renal perfusion will be assessed using two non-invasive monitoring techniques: Doppler ultrasonography-derived Renal Resistive Index (RRI) and Near-Infrared Spectroscopy (NIRS)-derived renal regional oxygen saturation (rSO₂). Measurements will be obtained at predefined perioperative time points, including after induction of anesthesia, during pneumoperitoneum, before extubation, and during the early postoperative period. Perioperative changes in renal perfusion parameters will be analyzed and correlated with clinical variables such as intra-abdominal pressure, pneumoperitoneum duration, hemodynamic parameters, fluid administration, urine output, and postoperative renal function. The study also aims to investigate the relationship between intraoperative renal perfusion changes and the development of postoperative acute kidney injury. The findings may contribute to improved perioperative monitoring and optimization of renal perfusion during minimally invasive abdominal surgery.
Trial Details
NCT Number NCT07635160
Lead Sponsor Istanbul University - Cerrahpasa
Conditions Renal Perfusion, Minimally Invasive Surgical Procedures, Acute Kidney Injury
Enrollment 51 participants
Start Date 2026-01-07
Primary Completion 2027-01-07 (estimated)
Study Completion 2027-01-07 (estimated)
Updated on ClinicalTrials.gov 2026-06-09