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临床试验/NCT07841756
NCT07841756尚未招募不适用

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

First Affiliated Hospital of Guangxi Medical University6 个研究点 分布在 1 个国家目标入组 3,000 人开始时间: 2026年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
3,000
试验地点
6
主要终点
Dice Similarity Coefficient for Renal Tumor Segmentation

研究概览

简要总结

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.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Other

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •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.

排除标准

  • •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.

研究组 & 干预措施

Malignant renal tumor

Benign renal tumor

结局指标

主要结局

Dice Similarity Coefficient for Renal Tumor Segmentation

时间窗: 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.

次要结局

  • Classification Performance Metrics and Heterogeneity Impact Assessment(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)

研究者

发起方
First Affiliated Hospital of Guangxi Medical University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jiwen Cheng

Vice president of the First Affiliated Hospital of Guangxi Medical University

First Affiliated Hospital of Guangxi Medical University

研究点 (6)

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