Renal Stone
Conditions
Brief summary
This is an observational, international, multicenter, cohort study, prospectively collecting clinical data registry on consecutive patients with urinary stone undergoing ECIRS.
Detailed description
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.
Interventions
OTHERECIRS
Endoscopic Combined Intrarenal Surgery
Sponsors
Chinese University of Hong Kong
Study design
Observational model
CASE_ONLY
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Inclusion criteria
* Patients with urinary calculi * Undergoing Endoscopic Combined Intrarenal Surgery (ECIRS) * Agreed to consent for the study
Exclusion criteria
* Patients who have ECIRS for other conditions, such as urothelial cancer etc. * Patients who intraoperative record was incomplete. * Patients only have either PCNL or ureteroscopy done (not both)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Target Stone status | up to 1 year | The fragmentation rate of target stone |
| Treatment related complication | Thirty days after the operation | he 30-day complications will be graded according to the Clavien-Dindo classification |
Countries
Hong Kong
Contacts
Primary ContactChi Fai NG, MD
Outcome results
None listed