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Blood test may spare thousands from unnecessary colon surgery

NCT ID NCT07319104

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study will collect blood samples from 1,000 people with small colon growths to see if a liquid biopsy can accurately tell benign from malignant lesions and predict cancer spread to lymph nodes. Current methods often lead to unnecessary surgery. The goal is to create a biobank to validate blood-based markers that could guide safer, more precise treatment decisions.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 1,000 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jun 2026

An estimate. Start dates often move.

Expected to finish

Dec 2031

An estimate. End dates often move.

Lead sponsor

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

Eligible patients will be identified and recruited in gastroenterology consultations, within the investigating centers to which they will be referred as part of routine care.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show 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: * Patient of legal age (≥ 18 years) * Patient with a superficial colonic tumor refered for submucosal dissection * Patient included in the FECCo cohort (patients will be included concomitantly in FECCO-Biobank) * Patient wishing to participate in the FECCO-BioBank biological collection Exclusion Criteria: * Person with significant comorbidities preventing blood sampling * Patients with a distant metastasis detected by imaging * Person unable to read and write French * Person who have expressed their opposition to participating in this research after being informed by an investigator and having read the information sheet * Person not benefiting from a national health insurance scheme * Person under legal protection, guardianship or curatorship * Person participating in other study with an ongoing exclusion period

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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.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    12 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Civil Hospices of Lyon

    Lyon, 69003, France

  • Jean Mermoy Private Hospital

    Lyon, 69008, France

  • Saint Joseph Hospital

    Paris, 75014, France

  • University Hospital of Amiens

    Amiens, 80054, France

  • University Hospital of Bordeaux

    Bordeaux, 33604, France

  • University Hospital of Brest

    Brest, 29200, France

  • University Hospital of Dijon

    Dijon, 21079, France

  • University Hospital of Limoges

    Limoges, 87042, France

  • University Hospital of Montpellier

    Montpellier, 34095, France

  • University Hospital of Nancy

    Nancy, 54511, France

  • University Hospital of Nîmes

    Nîmes, 30029, France

  • University Hospital of Rennes

    Rennes, 35033, France

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