ClinicalTrials.Veeva

Menu

Observational Study of Subjects Having Routine Recurrence Screening for Bladder Cancer

P

Predictive Biosciences

Status

Completed

Conditions

Bladder Cancer Recurrence

Study type

Observational

Funder types

Industry

Identifiers

NCT00903240
PBS-001

Details and patient eligibility

About

The purpose of this study is to detect recurrent bladder cancer using a combination of protein and DNA biomarkers in urine

Enrollment

1,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Intact bladder
  • Scheduled for cystoscopy for transitional cell bladder cancer recurrence screening
  • Urine donated prior to cystoscopy, Bladder biopsy, chemotherapy, intravesical therapy, radiation or TUR
  • Must be willing to sign IRB approved informed consent

Exclusion criteria

  • History or current diagnosis of any cancer except transitional cell bladder cancer or basal cell cancer
  • Known diagnosis of any autoimmune disease or HIV, HCV or HBV
  • History or current TB or any other active infection
  • Subject has gross hematuria
  • Receiving chemotherapy, intravesical therapy or radiation within 30 days of enrollment
  • Any surgery except urologic within past 30 days

Trial contacts and locations

20

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems