- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05193656
Bladder Cancer Detection Using Convolutional Neural Networks (BLAInostic)
January 28, 2024 updated by: Zealand University Hospital
The investigators aim to experiment and implement various deep learning architectures to achieve human-level accuracy in Computer-aided diagnosis (CAD) systems.
In particular, the investigators are interested in detecting bladder tumors from CT urography scans and cystoscopies of the bladder in this project.
Study Overview
Detailed Description
The investigators aim to experiment and implement various deep learning architectures to achieve human-level accuracy in Computer-aided diagnosis (CAD) systems.
In particular, the investigators are interested in detecting bladder tumors from CT urography scans and cystoscopies of the bladder in this project.
The investigators want to classify bladder tumors as cancer, non cancer, high grade and low grade, invasive and non-invasive, with high sensitivity and low false positive rate using various convolutional neural networks (CNN).
This task can be considered as the first step in building CAD systems for bladder cancer diagnosis.
Moreover, by automating this task, the investigator scan significantly reduce the time for the radiologists to create large-scale labeled datasets of CT-urography scans and reduce the false-negative and positive that can happen due to human evaluation cystoscopies.
Study Type
Observational
Enrollment (Estimated)
5000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Nessn Azawi, phd
- Phone Number: 26393034
- Email: nesa@regionsjaelland.dk
Study Locations
-
-
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Roskilde, Denmark, 4000
- Recruiting
- Zealand University Hospital
-
Contact:
- Nessn H. Azawi, M.D.
- Phone Number: 004526393034
- Email: nesa@regionsjaelland.dk
-
Principal Investigator:
- Nessn Azawi, Ph.D
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Probability Sample
Study Population
Patients with micro or macroscopic hematuria
Description
Inclusion Criteria:
- Patients with first time hematuria
- Patients with the control program for previous bladder cancer
Exclusion Criteria:
- Patients with control cystoscope for noncancer suspected disease
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Detecting bladder tumor
Patients with hematuria, or previous bladder tumor
|
Detection of bladder tumor with help of Artificial intelligence
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Comparing standard technique to Machine Learning
Time Frame: 5 years
|
The accuracy of Machine learning to detect bladder cancer compared to standard cystoscopy
|
5 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Detecting accuracy of subtypes of bladder cancer
Time Frame: 5 years
|
The abelity of Machine Learning to identify high grad bladder cancer from low grad bladder cancer
|
5 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Nessn Azawi, phd, Zealand University Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 1, 2021
Primary Completion (Estimated)
June 1, 2026
Study Completion (Estimated)
June 1, 2026
Study Registration Dates
First Submitted
November 17, 2021
First Submitted That Met QC Criteria
January 14, 2022
First Posted (Actual)
January 18, 2022
Study Record Updates
Last Update Posted (Actual)
January 30, 2024
Last Update Submitted That Met QC Criteria
January 28, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- SJ-905
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.