Efficacy Study of a Urine DEK ELISA for Diagnosis of Bladder Cancer
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|ClinicalTrials.gov Identifier: NCT01563796|
Recruitment Status : Unknown
Verified September 2015 by Medical Diagnostic Laboratories, LLC.
Recruitment status was: Active, not recruiting
First Posted : March 27, 2012
Last Update Posted : September 24, 2015
|Condition or disease|
|Hematuria Dysuria Bladder Cancer|
Urine samples used in the study will be collected immediately prior to the urological evaluation procedure and stored at -80 oC. Urine samples will be sent to sponsor and remain at -80o C until analysis.
Clinical Data Collection:
All subject and clinical information will be recorded on the form in section 9.3. Enrollment Checklist and Case Report Form (CRF). Information regarding the history of hematuria and urine cytology will be recorded. In addition, non-identifying information including age, sex, race, smoking history, alcohol consumption, occupational exposure to chemicals or dyes, history of urologic disorder or disease, history of irritative voiding symptoms, history of urinary tract infection, history of pelvic irradiation, and analgesic abuse will be recorded. The Investigators will also be asked to provide information from the subjects' medical records for up to one (1) year after their enrollment and sample collection. In particular, diagnosis of TCC, other malignant diseases, or non-malignant urogenital conditions will be provided.
|Study Type :||Observational|
|Estimated Enrollment :||1000 participants|
|Observational Model:||Case Control|
|Official Title:||A Multi-Center Study to Evaluate the Safety and Efficacy of a Urine DEK ELISA in Diagnosis of Subjects With Bladder Cancer|
|Study Start Date :||March 2012|
|Actual Primary Completion Date :||March 2014|
|Estimated Study Completion Date :||December 2016|
subjects with hematuria, dysuria or other irritative voiding symptoms, without evidence of other causative factors such as infections or stones that are found to have a bladder tumor confirmed by histopathology
subjects with hematuria, dysuria or other irritative voiding symptoms, without evidence of other causative factors such as infections or stones that are found to NOT have a bladder tumor by histopathology or clinical observation.
- Histology [ Time Frame: Up to 1 year after cystoscopy/biopsy ]
- Cystoscopy [ Time Frame: up to 3 months after collection ]
- Cytology [ Time Frame: up to 3 months after collection ]
Biospecimen Retention: None Retained
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01563796
|United States, New York|
|Staten Island University Hospital|
|Staten Island, New York, United States, 10305|
|Study Director:||Jason Trama, PhD||Medical Diagnostic Laboratories, LLC|