About this trial
This prospective clinical study aims to evaluate preoperative, intraoperative, and postoperative characteristics of patients undergoing retrograde intrarenal surgery (RIRS) for urinary stone disease. A total of approximately 250 patients will be assessed to identify clinical, laboratory, and operative factors associated with postoperative fever and sepsis. By systematically collecting and analyzing perioperative data, the study seeks to determine independent predictors that may support improved risk stratification and patient safety in endourological practice.
Eligibility criteria
Qualifiers
Age 18 years or older.
Patients scheduled to undergo retrograde intrarenal surgery (RIRS) for the treatment of renal or ureteral stones.
Completion of routine preoperative and postoperative clinical assessments required for RIRS.
Ability to provide informed consent.
Disqualifiers
Terminal-stage malignancy.
Bleeding diathesis or known immunodeficiency.
Active infectious condition at the time of surgery.
Patients deemed unsuitable for anesthesia or surgery by the Department of Anesthesiology.
Trial design
Treatments tested in this trial
- Not listed