Urinary Continence of Female POPRC and OIN (NCT05325216) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Urinary Continence of Female POPRC and OIN
China58 participantsStarted 2022-04
Plain-language 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.
Who can participate
Age range
55 Years – 75 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
. Female patients aged between 55-75.
. Patients those who are diagnosed with organ-confined urothelial carcinoma（\<pT3）
. Patients those who are capable for radical cystectomy with orthotopic ileal neobladder.
. ECOG score between 0-2;
. Normal renal function;
. Patients those who volunteer to participate in this study and sign the informed consents.
. Patients those who are able to cooperate in the study.
Exclusion criteria
. Absence of tumour in bladder neck or urethra;
. Patients thsoe who are diagnosed distant metastasis before surgery.
. Previous history of malignancy of pelvic organs or surgical resection of pelvic organs;
. Patients those who are diagnosed with other malignancies.;
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
day-time and night-time continence rate
Timeframe: 6 months
Trial details
NCT IDNCT05325216
SponsorSun Yat-Sen Memorial Hospital of Sun Yat-Sen University