Study probes why some get false alarms on bowel cancer test
NCT ID NCT05329870
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aimed to find out if certain genes that affect bleeding can cause a false positive result on a stool test used to screen for colon cancer. Researchers planned to compare genetic markers in people who had a high test result but a normal colonoscopy with those who had normal results. The study was withdrawn before enrolling any participants, so no conclusions were reached.
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Study facts
What this study's own registry entry says, in plain language.
- Expected to start
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May 2022
An estimate. Start dates often move.
- Expected to finish
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Nov 2023
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study would aim to enrol 150 participants. This would be in a 1:4 ratio, meaning 30 participants would have had a normal colonoscopy and a qFIT \>10 µg Hb/g and 120 participants would have a normal colonoscopy and a qFIT \<10 µg Hb/g.
- Ages
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16 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients who were symptomatic at the time of referral * Returned at least one qFIT sample * Underwent a complete colonoscopy, which did not identify any pathology * Willing to provide a saliva sample for genetic analysis * Are able to consent to the study Exclusion Criteria: * Age \< 18 * Previous colorectal cancer * Ongoing colonic polyp surveillance * Known inflammatory bowel disease * Taking anticoagulant medication (Aspirin, clopidogrel, warfarin or NOAC) * History of liver disease or known bleeding disorder * Incomplete colonoscopy * Unable to consent to the study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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NHS Lothian
Edinburgh, United Kingdom
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Other studies related to the condition(s) this trial covers.
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