RecruitingNot Applicable

Triple Assay of Rectal Mucus in the Diagnosis of Colorectal Cancer

United Kingdom6,600 participantsStarted 2024-11-01

Plain-language summary

Development of a multiomics assay for use on OriColTM sampled rectal mucus for detection of cancer and significant polyps in symptomatic patients on the Colorectal Urgent Suspected Cancer pathway.

Who can participate

Age range

18 Years – 99 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Patients 18 years and over
. Patients referred from primary care to the 'urgent suspected cancer' CRC pathway during the study period.
. Patients who provide voluntary written informed consent to participate in the study.

Exclusion criteria

. Patients who are unable to undergo digital rectal examination (DRE).
. Patients with peri-anal/anal symptoms that may limit DRE and proctoscopy examination and it would be clinically inappropriate to attempt to assess these patients. This may include conditions such as:
. Current pregnancy or suspicion of pregnancy.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

TRIOMIC - 1

Timeframe: 26 months

TRIOMIC - 2

Timeframe: 26 month

TRIOMIC - 3

Timeframe: 26 months

Trial details

NCT IDNCT06649123

SponsorOrigin Sciences

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2026-04-01

Contact for this trial

Jon Lacy-Colson, FRCS

+44(0)1743261000 jon.lacy-colson@sath.nhs.uk

View on ClinicalTrials.gov More Colorectal Cancer trials