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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05779631
Other study ID # 2022-15859
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 6, 2023
Est. completion date December 2028

Study information

Verified date January 2024
Source Radboud University Medical Center
Contact A. G. van der Heijden, Dr.
Phone +31 (0)24 361 37 35
Email toine.vanderheijden@radboudumc.nl
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A two-arm multicenter randomised controlled trial, comparing progression free survival, time to definitive treatment and cost-effectiveness of the standard of care (TURBT) and mpMRI followed by same-day cystoscopic bladder biopsy for diagnosis of patients with suspicion of muscle-invasive bladder cancer.


Recruitment information / eligibility

Status Recruiting
Enrollment 360
Est. completion date December 2028
Est. primary completion date July 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients (18+ years of age) with clinically suspected MIBC, without lymph node or distant metastases, written informed consent Exclusion Criteria: - Unable or unwilling to undergo mpMRI - Unfit for TURBT - Unfit for definitive treatment with curative intent - A history of cancer, including bladder cancer, except non-melanoma skin cancer or prostate cancer on active surveillance

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
mpMRI plus a same-day cystoscopic bladder biopsy
mpMRI plus a same-day cystoscopic bladder biopsy
Procedure:
TURBT
Transurethral resection of the bladder tumor

Locations

Country Name City State
Netherlands Ziekenhuisgroep Twente Almelo
Netherlands Amsterdam UMC, location AMC Amsterdam
Netherlands Amsterdam UMC, location VUmc Amsterdam
Netherlands Antoni van Leeuwenhoek - Netherlands Cancer Institute Amsterdam
Netherlands Maasziekenhuis Pantein Boxmeer
Netherlands Ziekenhuis Gelderse Vallei Ede
Netherlands St. Antonius ziekenhuis Nieuwegein
Netherlands Canisius Wilhelmina Ziekenhuis Nijmegen
Netherlands Radboud university medical center Nijmegen
Netherlands Erasmus Medical Center Rotterdam
Netherlands Bernhoven ziekenhuis Uden
Netherlands University Medical Center Utrecht Utrecht

Sponsors (1)

Lead Sponsor Collaborator
Radboud University Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Progression free survival Progression-free survival, defined as the time between randomisation and one of the following events, whichever occurs first:
Diagnosis of distant metastases
Diagnosis of loco-regional nodal recurrence
Death from any cause
2 years
Secondary Time to definitive treatment Definitive treatment is defined as TURBT in case of NMIBC and radical cystectomy with or without neoadjuvant chemotherapy or chemoradiotherapy in case of MIBC. Time to definitive treatment is the time between randomisation and the first of these mentioned treatments. 2 years
Secondary Health-related quality of life Generic health-related quality of life will be assessed at baseline, 6 months, 12 months and 24 months using the EuroQol 5 dimensions 5 levels (EuroQol 5D) questionnaire. 2 years
Secondary Hospital-related healthcare costs Hospital registries will be used to identify all items / procedures / activities related to the management of the bladder cancer and obtain a valid and reliable estimate of the costs. Unit costs will be based on the Dutch manual for costing studies. 2 years
Secondary Cost-effectiveness Unit costs will be based on the Dutch manual for costing studies. Effectiveness will be measured in terms of quality-adjusted life years (QALYs), following the Dutch guideline for economic evaluation (EuroQol 5D). 2 years
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