- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06172049
Incidence of Colorectal Cancer in Southwest China: Based on SCC Database
December 14, 2023 updated by: Ziqiang Wang,MD, West China Hospital
To evaluate recent trends in CRC incidence, treatment, and survival in the Southwest China.
Study Overview
Detailed Description
The epidemiological feature of colorectal cancer (CRC) showed different trends among countries.
Studying the epidemiological and management characteristics between China and the US has important implications for understanding the current status of cancer occurrence, treatment and survival.
we established the Southwest China Colorectal (SCC) database, aiming to provide reference information on the diagnosis and management of CRC in China.
Study Type
Observational
Enrollment (Actual)
5838
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
-
-
Sichuan
-
Chendu, Sichuan, China, 640001
- West China Hospital
-
-
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
All patients who were diagnosed with CRC were included
Description
Inclusion Criteria:
- Clinical diagnosis of colorectal cancer;
- Received treatment in medical institutions;
- Regular follow-up after the diagnosis.
Exclusion Criteria:
Patients who lost to follow-up
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 |
Intervention / Treatment |
|---|---|
|
CRC cases
|
the actual treatment CRC patients have reveived
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Survival
Time Frame: From inclusion until date of death from any cause, or untile the 2023-10-31
|
Overall survival (OS) untile the end of follow up
|
From inclusion until date of death from any cause, or untile the 2023-10-31
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Ziqiang Wang, West China 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)
January 1, 2014
Primary Completion (Actual)
December 31, 2017
Study Completion (Actual)
October 31, 2023
Study Registration Dates
First Submitted
December 6, 2023
First Submitted That Met QC Criteria
December 14, 2023
First Posted (Estimated)
December 15, 2023
Study Record Updates
Last Update Posted (Estimated)
December 15, 2023
Last Update Submitted That Met QC Criteria
December 14, 2023
Last Verified
December 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CRC-2023
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
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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