- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06537037
Exploring the Association of Imaging and Tumor Microenvironment in Urologic Cancer Using Radiogenomic Approach(Radiogenomics-Urinary)
July 31, 2024 updated by: Wuhan Union Hospital, China
This is the prospective, observational cohort study (Radiogenomics-Urinary), which aims to explore the relationship between the imaging information of urologic cancer patients, tumor microenvironment and the prognosis of urologic cancer patients.
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
150
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Lian Yang
- Phone Number: 18986273791
- Email: yanglian@hust.edu.cn
Study Locations
-
-
Hubei
-
Wuhan, Hubei, China, 430000
- Recruiting
- Union Hospital,Tongji Medical College,Huazhong University of Science and Technology
-
Contact:
- Lian Yang
- Phone Number: 18986273791
- Email: yanglian@hust.edu.cn
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients treated for urologic cancer
Description
Inclusion Criteria:
- Patients treated for urologic cancer in Wuhan Union Hospital from August 2024 to August 2027;
- Aged > 18 years old;
- At least one CT scan or MRI scan before treatment;
- Tissue biopsy pathological examination confirmed the diagnosis of the above tumors.
Exclusion criteria:
- Poor image quality;
- Incomplete clinical data or loss of follow-up;
- Presence of another primary malignancy other than urologic cancer;
- Unclear pathological diagnosis。
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Correlation analysis of sequencing results and body composition
Time Frame: 0.5 year
|
Conducting correlation analysis between body composition and results of multi-omics sequencing.
|
0.5 year
|
|
Correlation analysis of sequencing results and tumor radiomic features
Time Frame: 0.5 year
|
Conducting correlation analysis between radiomic features and results of multi-omics sequencing.
|
0.5 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Constructing tumor microenvironment prediction model
Time Frame: 2 years
|
Constructing radiomic model to predict tumor microenvironment.
The indicator is the area under the curve (AUC) of the prediction model
|
2 years
|
|
Constructing a multi-dimensional prognostic prediction model
Time Frame: 3 years
|
A high-dimensional model was constructed to predict the prognosis of patients through multi-omics sequencing data, body composition, and tumor radiomic features.
The indicator is the area under the curve (AUC) of the prediction model.
|
3 years
|
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 (Estimated)
August 1, 2024
Primary Completion (Estimated)
August 1, 2027
Study Completion (Estimated)
August 1, 2027
Study Registration Dates
First Submitted
July 31, 2024
First Submitted That Met QC Criteria
July 31, 2024
First Posted (Estimated)
August 5, 2024
Study Record Updates
Last Update Posted (Estimated)
August 5, 2024
Last Update Submitted That Met QC Criteria
July 31, 2024
Last Verified
July 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- S187
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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