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Diagnostic Performance of the Vesical Imaging-Reporting and Data System (VI-RADS) in Detecting Muscle-invasive Bladder Tumour (MIBC) in Clinical Practice: Comparison With Transurethral Resection of Bladder Cancer (TURB) and Evaluation of Diagnostic Accuracy According to Tumour Location - Trial NCT06337591

Access comprehensive clinical trial information for NCT06337591 through Pure Global AI's free database. This phase not specified trial is sponsored by Istituto Nazionale di Ricovero e Cura per Anziani and is currently Completed. The study focuses on Bladder Cancer. Target enrollment is 20 participants.

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NCT06337591
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Trial Details
ClinicalTrials.gov โ€ข NCT06337591
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Diagnostic Performance of the Vesical Imaging-Reporting and Data System (VI-RADS) in Detecting Muscle-invasive Bladder Tumour (MIBC) in Clinical Practice: Comparison With Transurethral Resection of Bladder Cancer (TURB) and Evaluation of Diagnostic Accuracy According to Tumour Location

Study Focus

Bladder Cancer

VI-RADS

Observational

procedure

Sponsor & Location

Istituto Nazionale di Ricovero e Cura per Anziani

Ancona,Ancona,Jesi, Italy

Timeline & Enrollment

N/A

Oct 15, 2022

Mar 10, 2024

20 participants

Primary Outcome

Sensitivity of Vescical Imaging-Reporting and Data System (VI-RADS) in predicting muscle-invasive bladder cancer after transurethral resection

Summary

VI-RADS was an observational, prospective, multicenter, no profit study. The aim of the study
 was to clarify the clinical validity of the Vesical Imaging-Reporting and Data System
 (VI-RADS) for the assessment of muscle invasion (MI) status in comparison with transurethral
 resection of bladder cancer (TURB) and to evaluate the diagnostic accuracy of the score
 according to the specific tumour location.

ICD-10 Classifications

Malignant neoplasm of bladder
Malignant neoplasm: Bladder, unspecified
Malignant neoplasm: Dome of bladder
Malignant neoplasm: Overlapping lesion of bladder
Malignant neoplasm: Lateral wall of bladder

Data Source

ClinicalTrials.gov

NCT06337591

Non-Device Trial