Targeted Decision Making In Renal Cell Carcinoma Relying on a Radiogenomics Translational Platform
NCT06868927
Adenocarcinoma, Carcinoma
Milan, Italia, Italy
View Trial DetailsNCT Number: NCT07841756
This is a multicenter, retrospective and prospective diagnostic clinical trial evaluating the effectiveness and safety of CascadeDiagnose Renal Tumor CT, an AI-assisted detection system for renal tumors based on contrast-enhanced multiphase CT imaging. The system employs a cascaded deep learning architecture to perform fully automated analysis of multiphase CT images, covering image quality review, lesion detection and segmentation, benign-malignant differentiation, and risk stratification, with traceable evidence chains and interpretable outputs. The study is conducted across six tertiary hospitals in Guangxi, China, utilizing a distributed "data stays on-site, computation moves across centers" federated learning network, which ensures that original patient data remain within each hospital while encrypted intermediate features are shared for cross-center collaborative analysis. A total of at least 3000 patients with renal tumors will be enrolled (approximately 2600 in the retrospective phase and 400 in the prospective phase). The primary effectiveness outcomes include area under the receiver operating characteristic curve (AUC), sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV). The primary safety outcomes include false negative rate, false positive rate, and adverse events. The study also incorporates a multi-reader, multi-case (MRMC) design to compare the diagnostic performance of the AI system with radiologists of varying seniority, and to evaluate the system's utility in assisting junior radiologists. The findings of this study are expected to provide high-quality clinical evidence for the regulatory approval of this AI-assisted diagnostic system as a Class III medical device.
Trial opening soon.
Get Notified18 year–60 year
All sexes
Observational
Guigang People's Hospital, Guigang, Guangxi, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: The primary outcome will be measured in October 2027, upon completion of model training, final parameter aggregation, and ensemble model establishment, using the test set from the multi-center retrospective cohort.
The primary outcome measure is the Dice Similarity Coefficient for renal tumor segmentation on contrast-enhanced CT, comparing the federated learning model against a centralized training model with a non-inferiority margin of Δ = -0.05. This outcome will be assessed at the end of the model training phase using an independent multi-center test set.
Time frame: Assessed at the completion of the model training phase, approximately 18 months after study initiation, following final aggregation and ensemble construction, using the independent multi-center test set, with center-specific and subtype-specific analyses
The secondary outcomes are: (1) classification performance metrics-AUC, accuracy, sensitivity, and specificity-for benign versus malignant renal tumor discrimination, with pathological diagnosis as the reference; and (2) the impact of data heterogeneity on model performance, assessed by comparing Dice coefficients and AUC values across centers and pathological subtypes. All secondary outcomes will be evaluated at the completion of the model training phase, approximately 18 months after study initiation, after the final federated aggregation and ensemble model construction, using the independent multi-center test set, with center-specific and subtype-specific analyses performed thereafter.
Trial opening soon.
Get NotifiedFirst Affiliated Hospital of Guangxi Medical University
Other
Research on the Application of Federated Learning in the Construction of Deep Learning Models for Renal Tumor Imaging
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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