UrolithiasisStone, KidneyStone UreterComplication of Surgical Procedure
Study summary
The purpose of this registry is to collect data on patients who have undergone minimally invasive treatments for urinary system stone disease, including percutaneous nephrolithotomy (PCNL), shock wave lithotripsy (SWL), semi-rigid ureterorenoscopy (URS), and flexible ureterorenoscopy (F-URS).
Eligibility
Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* To have a medical indication for urolithiasis
* Complete data of treatment and follow-up course
* Patients with consent
* Patients \> 18 years-old
* Patients \< 18 years-old
Exclusion Criteria:
* Missing data
* Patients without consent
* Not to have a medical indication for urolithiasis treatment
* To have a contraindication for urolithiasis treatment
Primary outcome measure(s)
Operative durations of each treatment technique (PCNL, SWL, URS, F-URS) — Operation/procedure day The duration of the operation time
Operative radiation dosage of each treatment technique (PCNL, SWL, URS, F-URS) — Operation/procedure day X-ray dosage
Operative results of each treatment technique (PCNL, SWL, URS, F-URS) — Operation/procedure day The duration of the laser time
Rate of postoperative complication — up to 3 months, postoperatively Abnormal clinical and laboratory findings that may be seen after surgery and require additional intervention, treatment, or follow-up
Follow-up — up to 10 years Follow-up results of patients for recurrence of disease of residual stones, if any reoperation records.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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