FITting Non-invasive Tests in Lynch Syndrome Surveillance

Part of paid clinical trials in Chicago, Illinois.

Sponsor
University of Chicago
Study ID
NCT06898996
Status
Recruiting
Apply to this trial

Conditions

Eligibility Criteria

Sex
ALL
Age
20 Years - 80 Years
Healthy Volunteers
Not accepted

Interventions

  • Fecal immunochemical test — OTHER
    Detects blood in stool

Study Details

The purpose of this clinical study is to evaluate the accuracy of the fecal immunochemical test (FIT) in comparison to colonoscopy in patients with Lynch Syndrome (LS) who are undergoing colonoscopy surveillance.

Key Dates

Start date
Jul 10, 2025
Status verified
Apr 2026
Primary completion
Mar 1, 2029
Completion
Jul 1, 2029

Study Design

Enrollment
400 participants (estimated)

Arms

  • Arm: Non-invasive surveillance test
    Easily accessible, affordable and acceptable tests can be used to triage Lynch syndrome patients to colonoscopy

Primary Outcome Measure

Quantitative Measure of specificity [ Time Frame: baseline -12 months ]

Central Contacts

Locations (3)

FacilityCityStateZIPSite coordinators
The University of Chicago Medical CenterChicagoIllinois60639
Sonia Kupfer, MD
[email protected]
773-834-1438
University of MichiganAnn ArborMichigan48109
Elena Stoffel, MD
[email protected]
734-647-7558
Columbia UniversityNew YorkNew York10032
Fay Kastrinos, MD
[email protected]
212-305-1021

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