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出境医 / 临床实验 / UroX Biomarker Bladder Cancer Study

UroX Biomarker Bladder Cancer Study

Study Description
Brief Summary:

This is a prospective observational study looking at urine samples from participants under referral for a standard of care investigative cystoscopy and biopsy.

The study aims to test if the UroX™ biomarker (a measurable indicator of a biological condition) can be detected in urine samples from participants who may later test positive following a biopsy for bladder cancer. The study aims to assess the value of the biomarker as a screening tool for bladder cancer.

Patients with and those without bladder cancer are required for the study.


Condition or disease Intervention/treatment
Bladder Cancer Diagnostic Test: UroX bladder cancer biomarker test

Detailed Description:

Patients who undergo investigation for bladder cancer will have a cystoscopy and biopsy as part of their routine care. These patients are then brought back to urology outpatient clinic for their biopsy results within two weeks.

A UroX Biomarker Bladder Cancer Study patient information leaflet will be sent to all patients who are booked for these investigations, explaining the study aims and the requirements for participation.

On the day of their cystoscopy, potential participants will be approached and after signing a study specific consent form, the urine sample will be accepted, given a study number and sent for UroX biomarker testing.

These results will then be returned to the study team for comparison against the biopsy histology result to assess for sensitivity and specificity.

While cystoscopy and biopsy are the current gold standard for diagnosis of bladder cancer, it has been shown to have false-negatives of between 10-40%, due to factors such as operator error or small areas of malignancy(15-17). The possibility of a screening/outpatient test for bladder cancer with high positive predictive value would help with reduction or prioritisation of further investigations and early diagnosis of disease thus potentially allowing alternative treatment options.

Study Design
Layout table for study information
Study Type : Observational
Estimated Enrollment : 100 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Evaluation of UroX™ Biomarker Screening Test in the Investigation of Bladder Cancer From Urine Samples - a Single Site Pilot Study
Actual Study Start Date : January 21, 2019
Estimated Primary Completion Date : July 1, 2020
Estimated Study Completion Date : July 1, 2025
Arms and Interventions
Group/Cohort Intervention/treatment
Participants with bladder cancer
50 participants with histologically confirmed evidence of malignancy for bladder cancer following routine cystoscopy and biopsy.
Diagnostic Test: UroX bladder cancer biomarker test
Urine test using novel UroX biomarker test for bladder malignancy

Participants without bladder cancer
50 participants with negative biopsy for bladder cancer following routine cystoscopy and biopsy.
Diagnostic Test: UroX bladder cancer biomarker test
Urine test using novel UroX biomarker test for bladder malignancy

Outcome Measures
Primary Outcome Measures :
  1. Evaluate the diagnostic accuracy of the UroX™ biomarker urine test [ Time Frame: 1 day (single visit/test) ]
    UroX™ urine biomarker staining result compared with standard of care biopsy result


Biospecimen Retention:   Samples Without DNA
Urine samples

Eligibility Criteria
Layout table for eligibility information
Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Participants under investigation for possible bladder cancer due to undergo cystoscopy and biopsy.
Criteria

Inclusion Criteria:

  • Patients aged ≥ 18 years of age
  • Patients under investigation for bladder cancer due to undergo investigative standard of care biopsy

Exclusion Criteria:

  • Patients aged < 18 years of age
  • Patients who are currently undergoing radiation therapy.
  • Proposed subject has no bladder (due to surgical removal).
  • No cystoscopy and/or pathology information for proposed subject (following cystoscopy for final inclusion in study results)
  • Patients unable or unwilling to provide consent
  • Patients currently on investigational drug trials
  • Patients with Catheter in Situ
Contacts and Locations

Contacts
Layout table for location contacts
Contact: Nikhil Vasdev 01438 28 4042 nikhil.vasdev@nhs.net
Contact: Alex Hampson 01438 28 4379 alexander.hampson@nhs.net

Locations
Layout table for location information
United Kingdom
East and North Hertfordshire NHS Trust Recruiting
Stevenage, Hertfordshire, United Kingdom, SG14AB
Contact: Nikhil Vasdev    01438 28 4042    nikhil.vasdev@nhs.net   
Sponsors and Collaborators
East and North Hertfordshire NHS Trust
KDx Diagnostics Inc.
Investigators
Layout table for investigator information
Principal Investigator: Nikhil Vasdev East and North Hertfordshire NHS Trust
Tracking Information
First Submitted Date June 1, 2019
First Posted Date June 4, 2019
Last Update Posted Date June 4, 2019
Actual Study Start Date January 21, 2019
Estimated Primary Completion Date July 1, 2020   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures
 (submitted: June 1, 2019)
Evaluate the diagnostic accuracy of the UroX™ biomarker urine test [ Time Frame: 1 day (single visit/test) ]
UroX™ urine biomarker staining result compared with standard of care biopsy result
Original Primary Outcome Measures Same as current
Change History No Changes Posted
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title UroX Biomarker Bladder Cancer Study
Official Title Evaluation of UroX™ Biomarker Screening Test in the Investigation of Bladder Cancer From Urine Samples - a Single Site Pilot Study
Brief Summary

This is a prospective observational study looking at urine samples from participants under referral for a standard of care investigative cystoscopy and biopsy.

The study aims to test if the UroX™ biomarker (a measurable indicator of a biological condition) can be detected in urine samples from participants who may later test positive following a biopsy for bladder cancer. The study aims to assess the value of the biomarker as a screening tool for bladder cancer.

Patients with and those without bladder cancer are required for the study.

Detailed Description

Patients who undergo investigation for bladder cancer will have a cystoscopy and biopsy as part of their routine care. These patients are then brought back to urology outpatient clinic for their biopsy results within two weeks.

A UroX Biomarker Bladder Cancer Study patient information leaflet will be sent to all patients who are booked for these investigations, explaining the study aims and the requirements for participation.

On the day of their cystoscopy, potential participants will be approached and after signing a study specific consent form, the urine sample will be accepted, given a study number and sent for UroX biomarker testing.

These results will then be returned to the study team for comparison against the biopsy histology result to assess for sensitivity and specificity.

While cystoscopy and biopsy are the current gold standard for diagnosis of bladder cancer, it has been shown to have false-negatives of between 10-40%, due to factors such as operator error or small areas of malignancy(15-17). The possibility of a screening/outpatient test for bladder cancer with high positive predictive value would help with reduction or prioritisation of further investigations and early diagnosis of disease thus potentially allowing alternative treatment options.

Study Type Observational
Study Design Observational Model: Cohort
Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Retention:   Samples Without DNA
Description:
Urine samples
Sampling Method Non-Probability Sample
Study Population Participants under investigation for possible bladder cancer due to undergo cystoscopy and biopsy.
Condition Bladder Cancer
Intervention Diagnostic Test: UroX bladder cancer biomarker test
Urine test using novel UroX biomarker test for bladder malignancy
Study Groups/Cohorts
  • Participants with bladder cancer
    50 participants with histologically confirmed evidence of malignancy for bladder cancer following routine cystoscopy and biopsy.
    Intervention: Diagnostic Test: UroX bladder cancer biomarker test
  • Participants without bladder cancer
    50 participants with negative biopsy for bladder cancer following routine cystoscopy and biopsy.
    Intervention: Diagnostic Test: UroX bladder cancer biomarker test
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Recruiting
Estimated Enrollment
 (submitted: June 1, 2019)
100
Original Estimated Enrollment Same as current
Estimated Study Completion Date July 1, 2025
Estimated Primary Completion Date July 1, 2020   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria:

  • Patients aged ≥ 18 years of age
  • Patients under investigation for bladder cancer due to undergo investigative standard of care biopsy

Exclusion Criteria:

  • Patients aged < 18 years of age
  • Patients who are currently undergoing radiation therapy.
  • Proposed subject has no bladder (due to surgical removal).
  • No cystoscopy and/or pathology information for proposed subject (following cystoscopy for final inclusion in study results)
  • Patients unable or unwilling to provide consent
  • Patients currently on investigational drug trials
  • Patients with Catheter in Situ
Sex/Gender
Sexes Eligible for Study: All
Ages 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers Yes
Contacts
Contact: Nikhil Vasdev 01438 28 4042 nikhil.vasdev@nhs.net
Contact: Alex Hampson 01438 28 4379 alexander.hampson@nhs.net
Listed Location Countries United Kingdom
Removed Location Countries  
 
Administrative Information
NCT Number NCT03973307
Other Study ID Numbers RD2018-68
Has Data Monitoring Committee No
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
IPD Sharing Statement
Plan to Share IPD: No
Responsible Party East and North Hertfordshire NHS Trust
Study Sponsor East and North Hertfordshire NHS Trust
Collaborators KDx Diagnostics Inc.
Investigators
Principal Investigator: Nikhil Vasdev East and North Hertfordshire NHS Trust
PRS Account East and North Hertfordshire NHS Trust
Verification Date June 2019

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