Lynch Syndrome X-Talk of Enteral Mucosa With Immune System

Recruiting Observational Study
Lynch Syndrome Lynch Syndrome I Lynch Syndrome II Lynch Syndrome I (Site-specific Colonic Cancer) HNPCC HNPCC Gene Mutation Hereditary Cancer Syndrome Hereditary Cancer MLH1 Gene Mutation MLH1 Gene Deletion+Duplication MLH1 Loss of Expression MLH1 Gene Inactivation MSH2 Gene Mutation MSH2 Gene Deletion+Duplication MSH2 Loss of Expression MSH2 Gene Inactivation MSH6 Gene Mutation MSH6 Loss of Expression MSH6 Gene Inactivation PMS2 Gene Mutation PMS2 Gene Inactivation PMS2 Loss of Expression
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
300 (estimated)
Sponsor
San Raffaele University · Other
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About This Trial
Lynch syndrome (OMIM #120435) is the most common dominantly inherited colorectal cancer syndrome with an estimated prevalence of 1:270 individuals. It increases the lifetime risk of colorectal and endometrial cancer primarily, but it is associated with a high risk of other cancers (pancreas, stomach, ovarian, central nervous system, skin, among others). It is caused by a germline mutation in one o…
Trial Locations
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Eligibility Criteria
Inclusion Criteria (for participants with Lynch syndrome): * Age ≥18 years * All sexes eligible * Established diagnosis of Lynch syndrome performed as part of clinical practice, with a germline pathogenic/likely pathogenic variant in one of the following genes: MLH1, MSH2, MSH6, PMS2, and EpCAM * S…
Contacts

Giulia Martina Cavestro, MD, PhD

0226436303

cavestro.giuliamartina@hsr.it

CONTACT

Alessandro Mannucci, MD

0226436303

mannucci.alessandro@hsr.it

CONTACT