- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06729346
Is the Normal Looking Bladder Mucosa on WL Cystoscopy During TURBT Really Normal and Can NBI Detect Hidden Tumor
January 26, 2025 updated by: Azmat ullah, Armed Forces Institute of Urology, Rawalpindi
Can Narrow-band Imaging Detect CIS/tumor in Normally Looking Bladder Mucosa on White Light Cystoscopy During Transurethral Resection of Bladder Tumor?
As every urologist does transurethral resection of bladder tumor.
So there are instances in which the operating surgeon is not sure whether the normal-looking mucosa or the inflammatory changes are really benign or if we are missing the CIS/bladder cancer.
Study Overview
Status
Recruiting
Conditions
Detailed Description
This is basically the observational study. in which we want to clarify that the normal-looking mucosa on white light cystoscopy is normal in reality or we are missing CIS/bladder tumor.
Study Type
Observational
Enrollment (Estimated)
100
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: azmat ullah, consultant urologist
- Phone Number: +923329354338
- Email: azmatdawar254@gmail.com
Study Contact Backup
- Name: ullah
- Email: azmatdawar254@gmail.com
Study Locations
-
-
Punjab
-
Rawalpindi, Punjab, Pakistan, 46000
- Recruiting
- Armed Forces Institute of Urology
-
Contact:
- azmat ullah, consultant urologist
- Phone Number: +923329354338
- Email: azmatdawar254@gmail.com
-
Contact:
- azmat ullah
-
Rawalpindi, Punjab, Pakistan, 46020
- Recruiting
- Armed Forces Institute of Urology
-
Contact:
- azmat ullah
- Phone Number: +923329354338
- Email: azmatdawar254@gmail.com
-
Contact:
- azmat ullah, consultant urologist
- Phone Number: +923329354338
- Email: azmatdawar254@gmail.com
-
Contact:
- azmat ullah, consultant urologist
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Probability Sample
Study Population
any patient who presented with armed forces institute of urology with bladder tumor .
Description
Inclusion Criteria:
any patient with bladder tumor
-
Exclusion Criteria:
- any patient whose age is less than 18 years any patient whose age is more than 75 years
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
to prove suspicious-looking mucosa on NBI has a bladder tumor on histopathology..
Time Frame: At the time of TURBT
|
At the time of TURBT
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: azmat ullah, consultant urologist, Armed Forces Institute of Urology
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)
December 28, 2024
Primary Completion (Estimated)
March 30, 2025
Study Completion (Estimated)
March 30, 2025
Study Registration Dates
First Submitted
December 7, 2024
First Submitted That Met QC Criteria
December 10, 2024
First Posted (Actual)
December 11, 2024
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 26, 2025
Last Verified
December 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Trg-1/IRB/2024/023
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Histopathology report
IPD Sharing Time Frame
01 January 2024 till 30 march 2024
IPD Sharing Access Criteria
each and everyone
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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.
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