- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06088134
Contrast-enhanced CT-based Deep Learning Model for Preoperative Prediction of Disease-free Survival (DFS) in Localized Clear Cell Renal Cell Carcinoma (ccRCC)
May 27, 2025 updated by: Mingzhao Xiao
Urology Department of the First Affiliated Hospital of Chongqing Medical University
This study aims to preoperatively predict DFS of patients with localised ccRCC using a deep learning prognostic model based on enhanced contrast CT images, validate it's predictive ability in multicentre data and compare it's predictive ability with traditional models.
Study Overview
Status
Recruiting
Study Type
Observational
Enrollment (Estimated)
800
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Chongqing
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Chongqing, Chongqing, China, 400016
- Recruiting
- Yingjie Xv
-
Contact:
- Yingjie Xv
- Phone Number: 83-18725891425
- Email: xvyingjiecq@qq.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients admitted to urology departments at participating medical centres
Description
Inclusion Criteria:
- underwent partial/radical nephrectomies
- histologically diagnosed as ccRCC
- with complete clinical data and preoperative CT image data
Exclusion Criteria:
- with incomplete clinic-pathological data
- lack of preoperative contrast-enhanced CT images or the image quality was unsuitable for analysis
- who received pre-surgery neoadjuvant or adjuvant therapies
- with multiple renal tumors or/and had synchronous metastasis
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Non-recurrence group
|
|
Recurrence group
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
disease-free survival (DFS)
Time Frame: recruitment occurred between June 2013 and March 2020
|
the interval from the date of surgery to disease recurrence, all-cause mortality or the last visit
|
recruitment occurred between June 2013 and March 2020
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 1, 2022
Primary Completion (Estimated)
June 1, 2025
Study Completion (Estimated)
August 1, 2025
Study Registration Dates
First Submitted
October 12, 2023
First Submitted That Met QC Criteria
October 12, 2023
First Posted (Actual)
October 18, 2023
Study Record Updates
Last Update Posted (Actual)
May 31, 2025
Last Update Submitted That Met QC Criteria
May 27, 2025
Last Verified
May 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Urogenital Diseases
- Urogenital Neoplasms
- Neoplasms by Site
- Neoplasms
- Male Urogenital Diseases
- Kidney Diseases
- Urologic Diseases
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Neoplasms by Histologic Type
- Neoplasms, Glandular and Epithelial
- Adenocarcinoma
- Urologic Neoplasms
- Kidney Neoplasms
- Carcinoma
- Carcinoma, Renal Cell
Other Study ID Numbers
- DL-ccRCC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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