mpMRI Compared to Diagnostic TURBT in Patients With Suspected Muscle-Invasive Bladder Cancer
Launched by UNIVERSITY OF CALIFORNIA, IRVINE · Mar 21, 2024
Trial Information
Current as of September 02, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at two different ways to diagnose muscle-invasive bladder cancer (MIBC) to see which one is more accurate. The study will compare the results from a special type of imaging called multi-parametric magnetic resonance imaging (mpMRI) with the results from a procedure called transurethral bladder tumor resection (TURBT), where a doctor removes tissue from the bladder to check for cancer. The goal is to see if the mpMRI can provide clear and accurate information about the cancer stage, as well as how these methods affect patients’ quality of life.
To participate in this trial, individuals must be at least 18 years old and have been identified by their doctor as having suspected muscle-invasive bladder cancer based on an initial examination. They should also be able to understand the study and agree to participate by signing a consent form. Participants will undergo both the mpMRI and the TURBT procedure, and the study will monitor their experiences and outcomes. It’s important to note that people who have had certain treatments or surgeries recently, or those who cannot undergo the imaging or surgery for medical reasons, may not be eligible for this study.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Age 18 years old or greater at the time of consent.
- • Suspected muscle-invasive bladder cancer by tumor appearance on initial routine cystoscopy as determined by the UCI-affiliated urologist performing this procedure.
- • ECOG Performance Status of 0-3.
- • Patients must have the ability to understand and the willingness to sign a written informed consent document (prior to the initiation of the study and any study procedures).
- • Patients must be willing and able to comply with the scheduled visits, imaging plan, follow up plan, and other specified study procedures in the opinion of the Investigator.
- Exclusion Criteria:
- • Prior TURBT within 120 days of study entry.
- • Prior therapy for bladder cancer within 120 days of study entry.
- • Inability to tolerate mpMRI or associated contrast.
- • Inability to tolerate TURBT or associated anesthesia.
- • ECOG Performance Status of 4.
- • Female patient who is known to be pregnant or breastfeeding.
About University Of California, Irvine
The University of California, Irvine (UCI) is a leading research institution renowned for its commitment to advancing health and medical knowledge through innovative clinical trials. With a robust infrastructure for clinical research, UCI fosters interdisciplinary collaboration among its esteemed faculty and researchers, aiming to translate scientific discoveries into effective therapeutic solutions. The university prioritizes ethical standards and participant safety while addressing critical healthcare challenges across various fields, including cancer, neurology, and public health. UCI's dedication to excellence in research and education positions it as a pivotal contributor to the advancement of clinical science and patient care.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Orange, California, United States
Patients applied
Trial Officials
Nataliya Mar, MD
Principal Investigator
Chao Family Comprehensive Cancer Center
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported