Urinary Continence of Female POPRC and OIN
Condition(s) studied
Investigational drug(s) / intervention(s)
POPRC+OIN: Pelvic-organ preserving radical cystectomy with orthotopic ileal neobladder
SRC+OIN: Standard radical cystectomy with orthotopic ileal neobladder
Study summary
To compare the urinary continence rate and long-term oncological outcomes of pelvic-organ preserving radical cystectomy (POPRC) with orthotopic ileal neobladder (OIN) versus standard radical cystectomy(SRC) with OIN.
Eligibility
Primary outcome measure(s)
- day-time and night-time continence rate — 6 months
We will use pad-test to evaluate the urinary continence for patients
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Sun Yat-Sen Memorial Hospital | Guangzhou | Guangdong |
More Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University trials in China
Other trials for the same condition
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.
View NCT05325216 on ClinicalTrials.gov ↗ ← All trials in China