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NCT Number: NCT07841756

Federated Learning in Renal Tumor Model

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.

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Guigang People's Hospital, Guigang, Guangxi, China

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients pathologically confirmed as having renal tumors (either benign or malignant) by surgery or biopsy;
  • Underwent contrastenhanced renal CT before surgery or treatment;
  • CT images are of good quality and clearly depict the renal lesion contour;
  • Complete and traceable clinical and pathological data.

Exclusion criteria

  • Patients who did not undergo contrastenhanced CT before surgery, or only had noncontrast CT;
  • CT images with significant motion artifacts, metal artifacts, or excessive noise that impair lesion assessment;
  • Lesions too small (maximum diameter <1 mm) or not identifiable on imaging;
  • Patients who previously underwent partial or radical nephrectomy for renal tumors (except for recurrent/residual lesions);
  • Incomplete clinical data or pathological results.

Treatment and study plan

Primary outcomes

  1. Dice Similarity Coefficient for Renal Tumor Segmentation

    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.

Secondary outcomes

  1. Classification Performance Metrics and Heterogeneity Impact Assessment

    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.

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Sponsors and collaborators

Lead sponsor

First Affiliated Hospital of Guangxi Medical University

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Registry information

Official study title

Research on the Application of Federated Learning in the Construction of Deep Learning Models for Renal Tumor Imaging

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Sep 25, 2026
Registry last updated
Sep 25, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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