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RECRUITINGOBSERVATIONAL

Prospective Sample Collection for Cancer of Bladder

Flemish Prospective Clinical and Pathological Database for Urothelial Cancer

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

The goal of the Flemish Databank for Urothelial Cancer is to collect clinical and pathological data of patients treated for urothelial cancer (UC).

Who May Be Eligible (Plain English)

Who May Qualify: - who are aged between 18-90, - who are of male or female sex, - who give their willing to sign a consent form to collect their clinical and pathological data, - who are planned to undergo TURBT for BC, - who are planned to undergo (salvage) radical cystectomy with or without an extended pelvic lymph node dissection, - who are planned to undergo tumor biopsy (from primary or metastatic tumor), - who are planned to undergo radical nephroureterectomy ± partial cystectomy or segmental ureterectomy, with or without a lymph node dissection, - who are planned to undergo endoscopic tumor biopsy or resection, - from whom metastases will be surgically removed. Who Should NOT Join This Trial: - patients who do not give their willing to sign a consent form to collect their clinical and pathological data, - patients who withdraw their willing to sign a consent form to use their clinical and pathological data, - patients who refuse the planned treatment, - women who are pregnant or have suspicion of pregnancy. Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * who are aged between 18-90, * who are of male or female sex, * who give their informed consent to collect their clinical and pathological data, * who are planned to undergo TURBT for BC, * who are planned to undergo (salvage) radical cystectomy with or without an extended pelvic lymph node dissection, * who are planned to undergo tumor biopsy (from primary or metastatic tumor), * who are planned to undergo radical nephroureterectomy ± partial cystectomy or segmental ureterectomy, with or without a lymph node dissection, * who are planned to undergo endoscopic tumor biopsy or resection, * from whom metastases will be surgically removed. Exclusion Criteria: * patients who do not give their informed consent to collect their clinical and pathological data, * patients who withdraw their informed consent to use their clinical and pathological data, * patients who refuse the planned treatment, * women who are pregnant or have suspicion of pregnancy.

Locations (1)

University Hospitals Leuven
Leuven, Vlaams-Brabant, Belgium