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NCT06582914Possibly a fitRecruiting

Lynch syndrome genetics and health study

Lynch Syndrome

Part of Cancer, Digestive system, Genetic & congenital, Hormones & metabolism clinical trials.

This study looks at the genetics and health of people with Lynch syndrome, a condition that raises the risk for certain cancers. Researchers want to learn more about how different genetic changes affect health over time.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
5,000 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You are 18 years old or older.
  • You have a genetic change (variant) in one of these genes: MLH1, MSH2, MSH6, PMS2, or EPCAM. This change could be a variant of uncertain significance (VUS), a pathogenic or likely pathogenic variant, or you are an obligate carrier of a pathogenic variant confirmed in your family.
  • Your genetic test result (from routine care) shows this specific variant.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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