This is an observational, international, multicenter, cohort study, prospectively collecting clinical data registry on consecutive patients with urinary stone undergoing ECIRS.
Patients diagnosed with urinary stones and planned for ECIRS in different centres will be recruited for the study. This registry collects clinical data on patients with ECIRS performed, includes baseline information on demography, symptoms, risk factors, and laboratory variables. Treatment information, perioperative outcomes, and follow-up details (up to 3 months after surgery) will also be collected. In summary, it captures patterns of presentation and treatment parameters, as well as perioperative and short-term outcomes of patients managed by ECIRS.
Study Type
OBSERVATIONAL
Enrollment
1,000
Endoscopic Combined Intrarenal Surgery
Alice Ho Miu Ling Nethersole Hospital
Hong Kong, Hong Kong
RECRUITINGPrince of Wales Hospital
Shatin, Hong Kong
RECRUITINGNorth District Hospital
Sheung Shui, Hong Kong
RECRUITINGTarget Stone status
The fragmentation rate of target stone
Time frame: up to 1 year
Treatment related complication
he 30-day complications will be graded according to the Clavien-Dindo classification
Time frame: Thirty days after the operation
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