- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07559825
Early-Onset Colorectal Cancer Patients Too Young for Screening
April 27, 2026 updated by: Methodist Health System
Early-Onset Colorectal Cancer Patients Too Young for Screening: Outcomes and Treatment Patterns
This is a population-based retrospective study using the Surveillance, Epidemiology, and End Results (SEER) registry and National Cancer Data Base (NCDB) to look at colorectal cancer (CRC) patients younger than 35 and comparing them against CRC patients older than 35 years of age.
Study Overview
Detailed Description
Specifically, investigator want to investigate the effect of having a diagnosis of CRC before the age of 35 years on:disease stage at presentation, insurance status at diagnosis, treatment patterns by stage, and adjusted cancer-specific survival.
The hypothesis is that patients younger than 35 years of age with CRC will present with more advanced disease at diagnosis but will have longer survival overall through more aggressive therapy.
Study Type
Observational
Enrollment (Estimated)
100
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: Crystee Cooper, DHEd
- Phone Number: 214-947-1280
- Email: ClinicalResearch@mhd.com
Study Contact Backup
- Name: Kavya Mankulangara
- Phone Number: 214-947-4604
- Email: ClinicalResearch@mhd.com
Study Locations
-
-
Texas
-
Dallas, Texas, United States, 75203
- Recruiting
- Methodist Dallas Medical Center- Clinical Research Institute
-
Contact:
- Kavya Mankulangara
- Phone Number: 214-947-4604
- Email: ClinicalResearch@mhd.com
-
Contact:
- Colette Ngo Ndjom
- Phone Number: 214-947-1289
- Email: ClinicalResearch@mhd.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
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Non-Probability Sample
Study Population
This is a population-based retrospective study using the Surveillance, Epidemiology, and End Results (SEER) registry and National Cancer Data Base (NCDB) to look at colorectal cancer (CRC) patients younger than 35 and comparing them against CRC patients older than 35 years of age.
Description
Inclusion Criteria:
- Colorectal cancer
Exclusion Criteria:
- No Colorectal cancer
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 |
|---|---|
|
colorectal cancer (CRC) patients younger than 35
The hypothesis is that patients younger than 35 years of age with CRC will present with more advanced disease at diagnosis but will have longer survival overall through more aggressive therapy.
|
CRC is a disease that is often associated with older adults (<50 years).
CRC remains the second most common cause of cancer death in males and the third most common cancer death in women.
Despite this, CRC incidence has steadily declined in older adults; however, there is a concerning rise of incidence of colorectal cancer in young patients.
The incidence of CRC in men and women under the age of 50 steadily increased 2.1 percent per year from 1992 through 2012.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Age
Time Frame: 20 years
|
colorectal cancer (CRC) patients younger than 35 years and comparing them against CRC patients older than 35 years of age.
|
20 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Rohan Jeyarajah, MD, Methodist Health System
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 31, 2020
Primary Completion (Estimated)
January 1, 2027
Study Completion (Estimated)
January 1, 2028
Study Registration Dates
First Submitted
March 18, 2026
First Submitted That Met QC Criteria
April 27, 2026
First Posted (Actual)
April 30, 2026
Study Record Updates
Last Update Posted (Actual)
April 30, 2026
Last Update Submitted That Met QC Criteria
April 27, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 036.HBP.2020.R
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
The data attained will be de-identified prior to sharing via presentation and/or publication in relevant research mediums.
IPD Sharing Time Frame
Not mentioned in protocol.
IPD Sharing Access Criteria
Not mentioned in protocol.
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.
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