Collection of Information to Better Understand Young Onset Colorectal Cancer

  • STATUS
    Recruiting
  • participants needed
    666
  • sponsor
    Memorial Sloan Kettering Cancer Center
Updated on 19 February 2024
adenocarcinoma
colorectal adenocarcinoma
inflammatory bowel disease
enteropathy
colorectal cancer

Summary

The purpose of this registry study is to create a databasea collection of informationfor better understanding young onset colorectal cancer. Colorectal cancer patients are considered to have young onset colorectal cancer if they are diagnosed with their cancer before the age of 50. Researchers will use the information from this database to learn more about how young onset colorectal cancer may be similar to or different from colorectal cancer that is diagnosed later in life. Researchers will also use information from the database for current and future research on young onset colorectal cancer.

Details
Condition Colorectal Cancer, Colorectal Cancer, Rectal disorder
Age 18-100 years
Treatment Risk Factor Questionnaire
Clinical Study IdentifierNCT04489238
SponsorMemorial Sloan Kettering Cancer Center
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Participant Inclusion Criteria for database and questionnaire (YOCRC)
Histological or cytological diagnosis of colorectal adenocarcinoma, confirmed at MSKCC
- 49 years old
No Known hereditary CRC syndrome (stool collection cohort only)
No history of inflammatory bowel disease ((stool collection cohort only)
No prior diagnosis of CRC (stool collection cohort only)
Participant Inclusion Criteria for database and questionnaire (Controls)
Histological or cytological diagnosis of colorectal adenocarcinoma, confirmed at MSKCC
No previous treatment for CRC (including surgery, chemotherapy, immunotherapy or radiation)
Age 50 or older
No Known hereditary CRC syndrome
No history of inflammatory bowel disease
No prior diagnosis of CRC
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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