- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06614179
A Pan-cancer Screening and Diagnosis Model Based on Abdominal CT Was Established
September 25, 2024 updated by: Xiangdong Cheng
Abdominal noncontrast scan and contrast-enhanced CT were used to establish a screening and diagnostic model for abdominal tumors
Study Overview
Status
Recruiting
Conditions
Detailed Description
Secondary objective: To establish a grading model of abdominal tumors based on clinical indicators Exploratory Objective: To include CT scans in large-scale non-tumor populations for validation and to improve model accuracy Certainty
Study Type
Observational
Enrollment (Estimated)
100000
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: Xiangdong Cheng
- Phone Number: 0086-571-881280
- Email: Chengxd516@126.com
Study Contact Backup
- Name: Can Hu
- Phone Number: 13968032995
- Email: chengxd@zjcc.org.cn
Study Locations
-
-
Zhejiang
-
Hangzhou, Zhejiang, China, 310000
- Recruiting
- Cancer Hospital of the University of Chinese Academy of Sciences (Zhejiang Cancer Hospital)
-
Contact:
- Xiangdong Cheng, PhD.
- Phone Number: +0086-0571-88128041
- Email: chengxd516@126.com
-
Hangzhou, Zhejiang, China, 310022
- Recruiting
- Zhejiang Cancer Hospital;Cancer hospital of the university of chinese academy of sciences
-
Contact:
- Pengfei Yu, MD,PhD
- Phone Number: +86-571-88128031
- Email: ypfzmu@163.com
-
Principal Investigator:
- Xiangdong Cheng, MD,PhD
-
Sub-Investigator:
- Yu Pengfei, MD,PhD
-
-
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
Yes
Sampling Method
Non-Probability Sample
Study Population
Patients with abdominal tumors or Non-tumor population
Description
Inclusion Criteria:
- Patients with abdominal tumors:
- all patients were pathologically diagnosed with abdominal tumors;
- The clinical case data of all patients were complete, and complete follow-up was obtained, with clear information on medical visits, operation time and survival status within 2 years. If the cause of death is unknown, it will be recorded as censored data;
- All patients had no history of active abdominal bleeding, no serious infection or other abdominal diseases that affected the observation of CT imaging within 3 months before surgery.
- Non-tumor population:
- all patients have complete clinical case data, complete abdominal CT, no history of malignant tumors, no serious infections or other abdominal diseases that affect the diagnosis and observation of CT imaging.
Exclusion Criteria:
- Cases in which contrast-enhanced or noncontrast CT images show unclear lesions, with significant noise and artifacts;
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 |
|---|---|---|
|
Whether or not there is a diagnosis of abdominal tumor questionnaire
Time Frame: first visited at baseline
|
Whether or not there is a diagnosis of abdominal tumor
|
first visited at baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Xiangdong Cheng, Zhejiang Cancer Hospital
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)
July 1, 2024
Primary Completion (Estimated)
December 31, 2029
Study Completion (Estimated)
December 31, 2029
Study Registration Dates
First Submitted
September 1, 2024
First Submitted That Met QC Criteria
September 25, 2024
First Posted (Actual)
September 26, 2024
Study Record Updates
Last Update Posted (Actual)
September 26, 2024
Last Update Submitted That Met QC Criteria
September 25, 2024
Last Verified
September 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IIT-2024-279
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Abdominal noncontrast scan and contrast-enhanced CT were used to establish a screening and diagnostic model for abdominal tumors
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
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.