RecruitingNot ApplicableNCT06989814
Smart Measurement of Circulating Tumor DNA
Smart Measurement of Circulating Tumor DNA: a Tumor-agnostic Computational Tool to Improve Colorectal Cancer Care
Sponsor
Erasmus Medical Center
Enrollment
50 participants
Start Date
May 16, 2025
Study Type
INTERVENTIONAL
Conditions
Summary
The goal of this study is to develop a blood-test which can detect colorectal cancer in early stages. Participants will be asked to take an extra blood test, which will be analyzed further in the lab.
Eligibility
Min Age: 18 Years
Inclusion Criteria4
- (suspect) Lynch Syndrome carriers who:
- Have proven Lynch Syndrome (MMR-gene or EPCAM mutation), or have a proven microsatellite instability high (MSI-H)tumor;
- Are at least 18 years old; Have been diagnosed with any form of cancer at the time of inclusion, but have had no treatment yet;
- Have granted informed consent to participate in this study.
Exclusion Criteria6
- (suspect) Lynch Syndrome carriers who:
- Are unwilling to undergo extra blood sampling;
- Are under the age of 18;
- Have no newly diagnosed tumors at time of inclusion;
- Have been treated for their tumor at time of inclusion;
- Are not able to read or understand Dutch language or are mentally not capable.
Interventions
DIAGNOSTIC_TESTBlood Product
An (extra) blood test will be done on participants. This will be analyzed for circulating tumor DNA (ctDNA) via a multi-omics approach.
Locations(2)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06989814
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