Bladder Bank (a Prospective Banking Study)

Overview

About this study

The purpose of this study is to establish samples (blood and urine) to support the development of non-invasive tests for early detection of bladder cancer 

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

- Age > 18 years

- Patient has undergone office-based evaluation for hematuria (computed tomography [CT],
ultrasound, cystoscopy)

Exclusion Criteria:

- Patient has known cancer outside of the target cancer 5 years prior to current
collection (not including basal cell or squamous cell skin cancers; if patient has not
been seen or if information is not available, the patient is eligible)

- Patient has recurrent muscle invasive bladder cancer

- Patient has ever been previously diagnosed with UTUC (upper tract urothelial
carcinoma) prior to bladder resection

- Patient has received chemotherapy class drugs for the treatment of non-target origin
cancer in the 5 years prior to current collection

- Patient has had any prior radiation therapy to the target lesion prior to current
collection

- Patient has had a biopsy to the target organ and/or lesion within 3 days before
collection

- Patient has undergone cystectomy

- Patient has transurethral instrumentation (placement of urinary catheter) within 7
days prior to urine collection

- Patient has had a urinary tract infection within 14 days prior to urine collection

- Patient has chronic indwelling urinary catheter

- Patient has prior diagnosis of bladder cancer for which prior resection of tumor was
performed

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 4/10/2024. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

John Kisiel, M.D.

Open for enrollment

Contact information:

Jacquelyn Arndt

(507) 266-3966

Arndt.Jacquelyn@mayo.edu

More information

Publications

Publications are currently not available
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CLS-20535180

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