A Novel Multiplex ELISA Assay for Surveilling Patients with History of Bladder Cancer

Status: Recruiting
Location: See all (4) locations...
Study Type: Observational
SUMMARY

Voided urinary cytology (VUC) is the most widely used urine-based assay for detecting bladder cancer (BCa); however, it fails to detect approximately 50% of low-grade or early stage BCa when it is most curable. Furthermore, the detection rate of VUC for recurrent BCa is not much better. Because of this severe limitation, all patients who are under surveillance to monitor for recurrent BCa must undergo an invasive examination of the urinary bladder, where a miniature camera is inserted into the bladder and the bladder inspected (cystoscopy). We propose to improve the non-invasive detection of recurrent BCa by further validating a multiplex ELISA assay directed at a BCa-associated diagnostic signature in voided urine samples.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

⁃ Participants must be:

• Age 18 years or older

• Have a history of non-muscle invasive bladder cancer or muscle invasive bladder cancer treated by bladder sparing techniques (or not yet treated) and diagnosed within the past 24 months on cystoscopic surveillance

• Participants may be treated with adjuvant intravesical therapy

• Willing and able to give written informed consent (see Appendix 1)

• Be willing to adhere to the surveillance regimen (high risk and intermediate risk seen every 3 months for 2 years; low risk seen every 6-12 months for 2 years)

Locations
United States
California
Cedars-Sinai Medical Center
RECRUITING
Los Angeles
University of California San Francisco
ACTIVE_NOT_RECRUITING
San Francisco
Texas
UT Southwestern Medical Center at Dallas
ACTIVE_NOT_RECRUITING
Dallas
Other Locations
Japan
Kyoto University Graduate School of Medicine
RECRUITING
Kyoto
Contact Information
Primary
Charles Rosser, MD
Charles.Rosser@cshs.org
310-423-5609
Time Frame
Start Date: 2016-12-30
Estimated Completion Date: 2026-02
Participants
Target number of participants: 300
Related Therapeutic Areas
Sponsors
Collaborators: Kyoto University, Fred Hutchinson Cancer Center, University of Texas, Nonagen Bioscience Corporation, National Cancer Institute (NCI), University of California, San Francisco
Leads: Cedars-Sinai Medical Center

This content was sourced from clinicaltrials.gov