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 |
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 |
| 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 |
| 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
|
| 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 |
Inclusion Criteria:
Exclusion Criteria:
| Contact: Nikhil Vasdev | 01438 28 4042 | nikhil.vasdev@nhs.net | |
| Contact: Alex Hampson | 01438 28 4379 | alexander.hampson@nhs.net |
| United Kingdom | |
| East and North Hertfordshire NHS Trust | Recruiting |
| Stevenage, Hertfordshire, United Kingdom, SG14AB | |
| Contact: Nikhil Vasdev 01438 28 4042 nikhil.vasdev@nhs.net | |
| 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 |
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
|
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| 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. |
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| 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. |
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| Study Type | Observational | ||||||||
| Study Design | Observational Model: Cohort Time Perspective: Prospective |
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| Target Follow-Up Duration | Not Provided | ||||||||
| Biospecimen | Retention: Samples Without DNA Description:
Urine samples
|
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| 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
|
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| Study Groups/Cohorts |
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| Publications * | Not Provided | ||||||||
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||||||
| Recruitment Status | Recruiting | ||||||||
| Estimated Enrollment |
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:
Exclusion Criteria:
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| Sex/Gender |
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| Ages | 18 Years and older (Adult, Older Adult) | ||||||||
| Accepts Healthy Volunteers | Yes | ||||||||
| Contacts |
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| 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 |
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| IPD Sharing Statement |
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| Responsible Party | East and North Hertfordshire NHS Trust | ||||||||
| Study Sponsor | East and North Hertfordshire NHS Trust | ||||||||
| Collaborators | KDx Diagnostics Inc. | ||||||||
| Investigators |
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| PRS Account | East and North Hertfordshire NHS Trust | ||||||||
| Verification Date | June 2019 | ||||||||